Moss genes from physcomitrella patens encoding proteins involved in the synthesis of amino acids, vitamins, cofactors, nucleotides and nucleosides

ABSTRACT

Isolated nucleic acid molecules, designated MP protein nucleic acid molecules, which encode novel MP proteins from e.g.  Phycomitrella patens  are described. The invention also provides antisense nucleic acid molecules, recombinant expression vectors containing MP protein nucleic acid molecules, and host cells into which the expression vectors have been introduced. The invention still further provides isolated MP proteins, mutated MP proteins, fusion proteins, antigenic peptides and methods for the improvement of production of a desired compound from transformed cells, organisms or plants based on genetic engineering of MP protein genes in these organisms.

BACKGROUND OF THE INVENTION

[0001] Certain products and by-products of naturally-occurring metabolic processes in cells have utility in a wide array of industries, including the food, feed, cosmetics, and pharmaceutical industries. These molecules, collectively termed ‘fine chemicals’, include organic acids, both proteinogenic and non-proteinogenic amino acids, nucleotides and nucleosides, lipids and fatty acids, diols and carbohydrates, aromatic compounds, vitamins and cofactors, and enzymes.

[0002] Their production is most conveniently performed through the large-scale culture of bacteria developed to produce and secrete large quantities of one or more desired molecules. One particularly useful organism for this purpose is Corynebacterium glutamicum, a gram positive, nonpathogenic bacterium.

[0003] Through strain selection, a number of mutant strains of the respective microorganisms have been developed which produce an array of desirable compounds. However, selection of strains improved for the production of a particular molecule is a time-consuming and difficult process.

[0004] Alternatively the production of fine chemicals can be most conveniently performed via the large scale production of plants developed to produce one of aforementioned fine chemicals. Of particular interest for this purpose are all crop plants for food and feed uses. Increased or modulated compositions of fone chemicals like amino acids, vitamins and nucleotides, in these plants would lead to optimized nutritional qualities.

[0005] Through conventional breeding, a number of mutant plants have been developed which produce increased amounts of for example, carotinoids, and amino acids. However, selection of new plant cultivars improved for the production of a particular molecule is a time-consuming and difficult process.

Summary of the Invention

[0006] This invention provides novel nucleic acid molecules which may be used to modify amino acids, vitamins, cofactors, nutraceuticals, nucleotides and nucleosides in plants, algae and microorganisms. Microorganisms like Corynebacterium, and fungi, and algae like Phaeodactylums are commonly used in industry for the large-scale production of a variety of fine chemicals.

[0007] Given the availability of cloning vectors for use in Corynebacterium glutamicum, such as those disclosed in Sinskey et al., U.S. Pat. No. 4,649,119, and techniques for genetic manipulation of C. glutamicum and the related Brevibacterium species (e.g., lactofermentum) (Yoshihama et al, J. Bacteriol. 162: 591-597 (1985); Katsumata et al., J. Bacteriol. 159: 306-311 (1984); and Santamaria et al., J. Gen. Microbiol. 130: 2237-2246 (1984)), the nucleic acid molecules of the invention may be utilized in the genetic engineering of this organism to make it a better or more efficient producer of one or more fine chemicals. This improved production or efficiency of production of a fine chemical may be due to a direct effect of manipulation of a gene of the invention, or it may be due to an indirect effect of such manipulation.

[0008] Given the availability of cloning vectors and techniques for genetic manipulation of ciliates such as disclosed in WO9801572 or algae and related organisms such as Phaeodactylum tricornutum described in Falciatore et al., 1999, Marine Biotechnology 1 (3):239-251 as well as Dunahay et al. 1995, Genetic transformation of diatoms, J. Phycol. 31:10004-1012 and references therein the nucleic acid molecules of the invention may be utilized in the genetic engineering of this organism to make it a better or more efficient producer of one or more fine chemicals. This improved production or efficiency of production of a fine chemical may be due to a direct effect of manipulation of a gene of the invention, or it may be due to an indirect effect of such manipulation.

[0009] The moss Physcomitrella patens represents one member of the mosses. It is related to other mosses such as Ceratodon purpureus which is capable to grow in the absense of light. Further Physcomitrella patens represents the only plant organism which can be utilized for targeted disruption of genes by homologous recombination. Mutants generated by this technique are useful to characterize the function for genes described in the invention. Mosses like Ceratodon and Physcomitrella share a high degree of homology on the DNA sequence and polypeptide level allowing the use of heterologous screening of DNA molecules with probes evolving from other mosses or organisms, thus enabling the derivation of a consensus sequence suitable for heterologous screening or functional annotation and prediction of gene functions in third species. The ability to identify such functions can therefor have significant relevance, e.g., prediction of substrate specificity of enzymes. Further, these nucleic acid molecules may serve as reference points for the mapping of moss genomes, or of genomes of related organisms.

[0010] These novel nucleic acid molecules encode proteins, referred to herein as metabolic pathway (MP) proteins. These MP proteins are capable of, for example, performing an enzymatic step involved in the metabolism of certain fine chemicals, including amino acids, vitamins, cofactors, nutraceuticals, nucleotides and nucleosides.

[0011] Given the availability of cloning vectors for use in plants and plant transformation, such as those published in and cited therein: Plant Molecular Biology and Biotechnology (CRC Press, Boca Raton, Fla.), chapter 6/7, S.71-119 (1993); F. F. White, Vectors for Gene Transfer in Higher Plants; in: Transgenic Plants, Vol. 1, Engineering and Utilization, eds.: Kung und R. Wu, Academic Press, 1993, 15-38; B. Jenes et al., Techniques for Gene Transfer, in: Transgenic Plants, Vol. 1, Engineering and Utilization, eds.: Kung und R. Wu, Academic Press (1993), 128-143; Potrykus, Annu. Rev. Plant Physiol. Plant Molec. Biol. 42 (1991), 205-225)) the nucleic acid molecules of the invention may be utilized in the genetic engineering of a wide variety of plants to make it a better or more efficient producer of one or more fine chemicals. This improved production or efficiency of production of a fine chemical may be due to a direct effect of manipulation of a gene of the invention, or it may be due to an indirect effect of such manipulation.

[0012] There are a number of mechanisms by which the alteration of an MP protein of the invention may directly affect the yield, production, and/or efficiency of production of a fine chemical in plant due to such an altered protein. The nucleic acid and protein molecules of the invention may directly improve the production or efficiency of production of one or more desired fine chemicals from Corynebacterium glutamicum, other microorganisms and plants. Using recombinant genetic techniques well known in the art, one or more of the biosynthetic or degradative enzymes of the invention for amino acids, vitamins, cofactors, nutraceuticals, nucleotides or nucleosides may be manipulated such that its function is modulated. For example, a biosynthetic enzyme may be improved in efficiency, or its allosteric control region destroyed such that feedback inhibition of production of the compound is prevented. Similarly, a degradative enzyme may be deleted or modified by substitution, deletion, or addition such that its degradative activity is lessened for the desired compound without impairing the viability of the cell. In each case, the overall yield or rate of production of the desired fine chemical may be increased.

[0013] It is also possible that such alterations in the protein and nucleotide molecules of the invention may improve the production of other fine chemicals besides the amino acids, vitamins, cofactors, nutraceuticals, nucleotide and nucleosides through indirect mechanisms. Metabolism of any one compound is necessarily interwined with other biosynthetic and degradative pathways within the cell, and necessary cofactors, intermediates, or substrates in one pathway are likely supplied or limited by another such pathway. Therefore, by modulating the activity of one or more of the proteins of the invention, the production or efficiency of activity of another fine chemical biosynthetic or degradative pathway may be impacted. For example, amino acids serve as the structural units of all proteins, yet may be present intracellularly in levels which are limiting for protein synthesis; therefore, by increasing the efficiency of production or the yields of one or more amino acids within the cell, proteins, such as biosynthetic or degradative proteins, may be more readily synthesized. Likewise, an alteration in a metabolic pathway enzyme such that a particular side reaction becomes more or less favored may result in the over- or under-production of one or more compounds which are utilized as intermediates or substrates for the production of a desired fine chemical.

[0014] Those MP proteins involved in the transport of fine chemical molecules from the cell may be increased in number or activity such that greater quantities of these compounds are allocated to different plant cell compartments or the cell exterior space from which they are more readily recovered and partitioned into the biosynthetic flux or deposited. Similarly, those MP protein involved in the import of nutrients necessary for the biosynthesis of one or more fine chemicals (e.g., amino acids, vitamins, cofactors, nutraceuticals, nucleotides and nucleosides) may be increased in number or activity such that these precursors, cofactors, or intermediate compounds are increased in concentration within the cell or within the storing compartments. The invention pertains to an isolated nucleic acid molecule which encodes an MP protein or an MP polypeptide involved in assisting in transmembrane transport.

[0015] The mutagenesis of one or more MP protein of the invention may also result in MP proteins having altered activities which indirectly impact the production of one or more desired fine chemicals from plants. For example, MP proteins of the invention involved in the export of waste products may be increased in number or activity such that the normal metabolic wastes of the cell (possibly increased in quantity due to the overproduction of the desired fine chemical) are efficiently exported before they are able to damage nucleotides and proteins within the cell (which would decrease the viability of the cell) or to interfere with fine chemical biosynthetic pathways (which would decrease the yield, production, or efficiency of production of the desired fine chemical). Further, the relatively large intracellular quantities of the desired fine chemical may in itself be toxic to the cell or may interfere with enzyme feedback mechanisms such as allosteric regulation, so by increasing the activity or number of transporters able to export this compound from the compartment, one may increase the viability of seed cells, in turn leading to a greater number of cells in the culture producing the desired fine chemical. The MP proteins of the invention may also be manipulated such that the relative amounts of different amino acids, vitamins, cofactors, nutraceuticals, nucleotides and nucleosides are produced. This can be appreciable for optimizing plant nutritional composition. Moreover such plants could be used for dietary purposes. For example a low level of purine nucleotides in the diet is a way to treat gout.

[0016] In plants these changes can moreover also influence other characteristic like tolerance towards abiotic and biotic stress conditions.

[0017] The invention provides novel nucleic acid molecules which encode proteins, referred to herein as MP proteins, which are capable of, for example, performing an enzymatic step involved in the metabolism of molecules important for the normal functioning of cells, such as amino acids, vitamins, cofactors, nucleotides and nucleosides. Nucleic acid molecules encoding an MP protein are referred to herein as MP protein nucleic acid molecules. In a preferred embodiment, the MP protein performs an enzymatic step related to the metabolism of one or more of the following: amino acids, vitamins, cofactors, nutraceuticals, nucleotides, nucleosides. Examples of such proteins include those encoded by the genes set forth in Table 1.

[0018] As biotic and abiotic stress tolerance is a general trait wished to be inherited into a wide variety of plants like maize, wheat, rye, oat, triticale, rice, barley, sorghum, potato, tomato, soybean, bean, pea, peanut, cotton, rapeseed, canola, alfalfa, grape, fruit plants (apple, pear, pinapple), bushy plants (coffee, cacao, tea), trees (oil palm, coconut), legumes, perennial grasses, and forage crops. These crop plants are also preferred target plants for a genetic engineering as one further embodiment of the present invention.

[0019] Accordingly, one aspect of the invention pertains to isolated nucleic acid molecules (e.g., cDNAs) comprising a nucleotide sequence encoding an MP protein or biologically active portions thereof, as well as nucleic acid fragments suitable as primers or hybridization probes for the detection or amplification of MP protein-encoding nucleic acid (e.g., DNA or mRNA). In another embodiment, the isolated nucleic acid molecule is at least 15 nucleotides in length and hybridizes under stringent conditions to a nucleic acid molecule comprising a nucleotide sequence of Appendix A. Preferably, the isolated nucleic acid molecule corresponds to a naturally-occurring nucleic acid molecule. More preferably, the isolated nucleic acid encodes a naturally-occurring Physcomitrella patens MP protein, or a biologically active portion thereof. In particularly preferred embodiments, the isolated nucleic acid molecule comprises one of the nucleotide sequences set forth in Appendix A or the coding region or a complement of one of these nucleotide sequences. In other particularly preferred embodiments, the isolated nucleic acid molecule of the invention comprises a nucleotide sequence which hybridizes to or is at least about 50%, preferably at least about 60%, more preferably at least about 70%, 80% or 90%, and even most preferably at least about 95%, 96%, 97%, 98%, 99% or more homologous to a nucleotide sequence set forth in Appendix A, or a portion thereof. In other preferred embodiments, the isolated nucleic acid molecule encodes one of the amino acid sequences set forth in Appendix B. The preferred MP proteins of the present invention also preferably possess at least one of the MP protein activities described herein.

[0020] In another embodiment, the isolated nucleic acid molecule encodes a protein or portion thereof wherein the protein or portion thereof includes an amino acid sequence which is sufficiently homologous to an amino acid sequence of Appendix B, e.g., sufficiently homologous to an amino acid sequence of Appendix B such that the protein or portion thereof maintains an MP protein activity. Preferably, the protein or portion thereof encoded by the nucleic acid molecule maintains the ability to perform an enzymatic reaction in a amino acid, vitamin, cofactor, nutraceutical, nucleotide, or nucleoside metabolic pathway. In one embodiment, the protein encoded by the nucleic acid molecule is at least about 50%, preferably at least about 60%, and more preferably at least about 70%, 80%, or 90% and most preferably at least about 95%, 96%, 97%, 98%, or 99% or more homologous to an amino acid sequence of Appendix B (e.g., an entire amino acid sequence selected from those sequences set forth in Appendix B). In another preferred embodiment, the protein is a full length Physcomitrella patens protein which is substantially homologous to an entire amino acid sequence of Appendix B (encoded by an open reading frame shown in Appendix A).

[0021] In another preferred embodiment, the isolated nucleic acid molecule is derived from Physcomitrella patens and encodes a protein (e.g., an MP protein fusion protein) which includes a biologically active domain which is at least about 50% or more homologous to one of the amino acid sequences of Appendix B and is able to perform an enzymatic reaction in a amino acid, vitamin, cofactor, nutraceutical, nucleotide or nucleoside metabolic pathway or has one or more of the activities set forth in Table 1, and which also includes heterologous nucleic acid sequences encoding a heterologous polypeptide or regulatory regions.

[0022] Another aspect of the invention pertains to an MP protein polypeptide whose amino acid sequence can be modulated with the help of art-known computer simulation programs resulting in an polypeptide with e.g. improved activity or altered regulation (molecular modeling). On the basis of this artificially generated polypeptide sequences, a corresponding nucleic acid molecule coding for such a modulated polypeptide can be synthesized in-vitro using the specific codon-usage of the desired host cell, e.g. of microorganisms, mosses, algae, ciliates, fungi or plants. In a preferred embodiment, even these artificial nucleic acid molecules coding for improved MP protein proteins are within the scope of this invention.

[0023] Another aspect of the invention pertains to vectors, e.g., recombinant expression vectors, containing the nucleic acid molecules of the invention, and host cells into which such vectors have been introduced, especially microorganims, plant cells, plant tissue, organs or whole plants. In one embodiment, such a host cell is a cell capable of storing fine chemical compounds in order to isolate the desired compound from harvested material The compound or the MP protein can then be isolated from the medium or the host cell, which in plants are cells containing and storing fine chemical compounds, most preferably cells of storage tissues like epidermal and seed cells.

[0024] Yet another aspect of the invention pertains to a genetically altered Physcomitrella patens plant in which an MP protein gene has been introduced or altered. In one embodiment, the genome of the Physcomitrella patens plant has been altered by introduction of a nucleic acid molecule of the invention encoding wild-type or mutated MP protein sequence as a transgene. In another embodiment, an endogenous MP protein gene within the genome of the Physcomitrella patens plant has been altered, e.g., functionally disrupted, by homologous recombination with an altered MP protein gene. In a preferred embodiment, the plant organism belongs to the genus Physcomitrella or Ceratodon, with Physcomitrella being particularly preferred. In a preferred embodiment, the Physcomitrella patens plant is also utilized for the production of a desired compound, such as amino acids, vitamins, cofactors, nutraceuticals, nucleotides and nucleosides. Hence in another preferred embodiment, the moss Physcomitrella patens can be used to show the function of new, yet unidentified genes of mosses or plants using homologous recombination based on the nucleic acids described in this invention.

[0025] Still another aspect of the invention pertains to an isolated MP protein or a portion, e.g., a biologically active portion, thereof. In a preferred embodiment, the isolated MP protein or portion thereof can catalyze an enzymatic reaction involved in one or more pathways for the metabolism of an amino acid, a vitamin, a cofactor, a nutraceutical, a nucleotide, or a nucleoside. In another preferred embodiment, the isolated MP protein or portion thereof is sufficiently homologous to an amino acid sequence of Appendix B such that the protein or portion thereof maintains the ability to catalyze an enzymatic reaction involved in one or more pathways for the metabolism of an amino acid, a vitamin, a cofactor, a nutraceutical, a nucleotide, or a nucleoside.

[0026] The invention also provides an isolated preparation of an MP protein. In preferred embodiments, the MP protein comprises an amino acid sequence of Appendix B. In another preferred embodiment, the invention pertains to an isolated full length protein which is substantially homologous to an entire amino acid sequence of Appendix B (encoded by an open reading frame set forth in Appendix A). In yet another embodiment, the protein is at least about 50%, preferably at least about 60%, and more preferably at least about 70%, 80%, or 90%, and most preferably at least about 95%, 96%, 97%, 98%, or 99% or more homologous to an entire amino acid sequence of Appendix B. In other embodiments, the isolated MP protein comprises an amino acid sequence which is at least about 50% or more homologous to one of the amino acid sequences of Appendix B and is able to perform an enzymatic reaction in a amino acid, vitamin, cofactor, nutraceutical, nucleotide or nucleoside metabolic pathway in a microorganism or a plant cell or has one or more of the activities set forth in Table 1.

[0027] Alternatively, the isolated MP protein can comprise an amino acid sequence which is encoded by a nucleotide sequence which hybridizes, e.g., hybridizes under stringent conditions, or is at least about 50%, preferably at least about 60%, more preferably at least about 70%, 80%, or 90%, and even most preferably at least about 95%, 96%, 97%, 98,%, or 99% or more homologous, to a nucleotide sequence of Appendix B. It is also preferred that the preferred forms of MP Proteins also have one or more of the MP Proteins activities described herein.

[0028] The MP protein, or a biologically active portion thereof, can be operatively linked to a non-MP protein polypeptide to form a fusion protein. In preferred embodiments, this fusion protein has an activity which differs from that of the MP protein alone. In other preferred embodiments, this fusion protein performs an enzymatic reaction in a amino acid, vitamin, cofactor, nutraceutical, nucleotide or nucleoside metabolic pathway. In particularly preferred embodiments, integration of this fusion protein into a host cell modulates production of a desired compound from the cell. Further, the instant invention pertains to an antibody specifically binding to an MP polypeptide mentioned before or to a portion thereof.

[0029] Another aspect of the invention pertains to a test kit comprising a nucleic acid molecule encoding an MP protein, a portion and/or a complement of this nucleic acid molecule used as probe or primer for identifying and/or cloning further nucleic acid molecules involved in the synthesis of amino acids, vitamins, cofactors, nucloetides and/or nucleosides or assisting in transmembrane transport in other cell types or organisms. In another embodiment the test kit comprises an MP protein-antibody for identifying and/or purifying further MP protein molecules or fragments thereof in other cell types or organisms.

[0030] Another aspect of the invention pertains to a method for producing a fine chemical. This method involves either the culturing of a suitable microorganism or culturing plant cells tissues, organs or whole plants containing a vector directing the expression of an MP protein nucleic acid molecule of the invention, such that a fine chemical is produced. In a preferred embodiment, this method further includes the step of obtaining a cell containing such a vector, in which a cell is transformed with a vector directing the expression of an MP protein nucleic acid. In another preferred embodiment, this method further includes the step of recovering the fine chemical from the culture. In a particularly preferred embodiment, the cell is from the genus Physcomitrella, Phaeodactylum, Corynebacterium, mosses, algae or plants.

[0031] Another aspect of the invention pertains to a method for producing a fine chemical which involves the culturing of a suitable host cell whose genomic DNA has been altered by the inclusion of an MP protein nucleic acid molecule of the invention. Further, the invention pertains to a method for producing a fine chemical which involves the culturing of a suitable host cell whose membrane has been altered by the inclusion of an MP protein of the invention.

[0032] Another aspect of the invention pertains to methods for modulating production of a molecule from a microorganism. Such methods include contacting the cell with an agent which modulates MP protein activity or MP protein nucleic acid expression such that a cell associated activity is altered relative to this same activity in the absence of the agent. In a preferred embodiment, the cell is modulated for one or more metabolic pathways for amino acids, vitamins, cofactors, nutraceuticals, nucleotides or nucleosides such that the yields or rate of production of a desired fine chemical by this microorganism is improved. The agent which modulates MP protein activity can be an agent which stimulates MP protein activity or MP protein nucleic acid expression. Examples of agents which stimulate MP protein activity or MP protein nucleic acid expression include small molecules, active MP proteins, and nucleic acids encoding MP proteins that have been introduced into the cell. Examples of agents which inhibit MP protein activity or expression include small molecules and antisense MP protein nucleic acid molecules.

[0033] Another aspect of the invention pertains to methods for modulating yields of a desired compound from a cell, involving the introduction of a wild-type or mutant MP protein gene into a cell, either maintained on a separate plasmid or integrated into the genome of the host cell. If integrated into the genome, such integration can be random, or it can take place by recombination such that the native gene is replaced by the introduced copy, causing the production of the desired compound from the cell to be modulated or by using a gene in trans such as the gene is functionally linked to a functional expression unit containing at least a sequence facilitating the expression of a gene and a sequence facilitating the polyadenylation of a functionally transcribed gene.

[0034] In a preferred embodiment, said yields are modified. In another preferred embodiment, said desired chemical is increased while unwanted disturbing compounds can be decreased. In a particularly preferred embodiment, said desired fine chemical can be decreased. In a particularly preferred embodiment, said desired fine chemical is an amino acid, vitamin, cofactor, nutraceutical, nucleotide or nucleoside.

[0035] Another aspect of the invention pertains to the fine chemicals produced by a method described before and the use of the fine chemical or a polypeptide of the invention for the production of another fine chemical.

DETAILED DESCRIPTION OF THE INVENTION

[0036] The present invention provides MP protein nucleic acid and protein molecules which are involved in the metabolism of amino acids, vitamins, cofactors, nutraceuticals, nucleotides and nucleosides in the moss Physcomitrella patens. The molecules of the invention may be utilized in the modulation of production of fine chemicals in microorganisms, algae and plants either directly (e.g., where overexpression or optimization of a vitamin biosynthesis protein has a direct impact on the yield, production, and/or efficiency of production of the vitamin from modified organisms), or may have an indirect impact which nonetheless results in an increase of yield, production, and/or efficiency of production of the desired compound or decrease of undesired compounds (e.g., where modulation of the metabolism of vitamins results in alterations in the yield, production, and/or efficiency of production or the composition of desired compounds within the cells, which in turn may impact the production of one or more fine chemicals).

[0037] Preferred mircroorganisms for the production or modulation of fine chemicals are for example Corynebacterium glutamicum, Sychenocystis spec., Sychenococcus spec., Ashbya gossypii, Neurospora crassa, Aspergillus spec., Saccharomyces cerevisiae. Preferred algae for the production or modulation of fine chemicals are Chlorella spec., Crypthecodineum spec., Phylodactenum spec. Preferred plants for the production or modulation of fine chemicals are for example mayor crop plants for example maize, wheat, rye, oat, triticale, rice, barley, sorghum, potato, tomato, soybean, bean, pea, peanut, cotton, rapeseed, canola, alfalfa, grape, fruit plants (apple, pear, pineapple), bushy plants (coffee, cacao, tea), trees (oil palm, coconut), legumes, perennial grasses, and forage crops.

[0038] Particularly suited for the production or modulation of lipophilic fine chemicals such as vitamins A and E and carotenoids are oil seed plants containing high amounts of lipid compounds like rapeseed, canola, linseed, soybean and sunflower.

[0039] Aspects of the invention are further explicated below.

[0040] Fine Chemicals

[0041] The term ‘fine chemical’ is art-recognized and includes molecules produced by an organism which have applications in various industries, such as, but not limited to, the pharmaceutical, agriculture, and cosmetics industries. Such compounds include lipids, fatty acids, vitamins, cofactors and enzymes, both proteinogenic and non-proteinogenic amino acids, purine and pyrimidine bases, nucleosides, and nucleotides (as described e.g. in Kuninaka, A. (1996) Nucleotides and related compounds, p. 561-612, in Biotechnology vol. 6, Rehm et al., eds. VCH: Weinheim, and references contained therein), lipids, both saturated and polyunsaturated fatty acids (e.g., arachidonic acid), diols (e.g., propane diol, and butane diol), carbohydrates (e.g., hyaluronic acid and trehalose), aromatic compounds (e.g., aromatic amines, vanillin, and indigo), vitamins and cofactors (as described in Ullmann's Encyclopedia of Industrial Chemistry, vol. A27, Vitamins, p. 443-613 (1996) VCH: Weinheim and references therein; and Ong, A. S., Niki, E. & Packer, L. (1995) Nutrition, Lipids, Health, and Disease” Proceedings of the UNESCO/Confederation of Scientific and Technological Associations in Malaysia, and the Society for Free Radical Research, Asia, held Sep. 1-3, 1994 at Penang, Malaysia, AOCS Press, (1995)), enzymes, and all other chemicals described in Gutcho (1983) Chemicals by Fermentation, Noyes Data Corporation, ISBN: 0818805086 and references therein. The metabolism and uses of certain of these fine chemicals are further explicated below.

[0042] Amino Acid Metabolism and Uses

[0043] Nutritional quality of crop plants is determined through their content of essential amino acids provided as protein source for food of humans or feed of monogastric animals, which are unable to synthesise these amino acids. Humans and animals can only synthesize 11 of the 20 amino acids. Essential amino acids are lysine, tryptophane, valine, leucine, isoleucine, methionine, threonine, phenylalanine, and histidine. Human and animal nutrition is mainly based upon plant components. However, often these amino acids are present only in very low concentrations in the plants or their seeds and fruits.

[0044] For this reason, grain mixtures and vegetable-based food have to be often supplemented with synthetically produced amino acids to increase the nutritional value.

[0045] The biosynthesis of essential amino acids is described in great detail by Michal G Ed. (1999, Biochemical Pathways, Spekrum Akademischer Verlag GmbH Heidelberg, and references cited therein). For additional review see Beach L R, Ballo B (1991, Curr. Top. Plant. Physiol. 7: 229-238). The biosynthesis of methionine, the only sulfur-containing amino acid that is essential for mammals is reviewed in Ravanel S, Gakiere B, Job D, Douce R (1998, Proc. Natl. Acad. Sci 95: 7805-7812).

[0046] Several attempts to positively influence amino acid metabolism by expression of biosynthetic genes were published recently (WO 9856935; EP 0854189; EP 0485970).

[0047] Plant genes originating from Physcomitrella patens can be used to modify metabolism of essential amino acids in plants as well as algae and microorganisms enabling these host cells and organisms to increase their capacity to produce amino acids as well as improving survival and fitness of the host cell.

[0048] Vitamin, Cofactor, and Nutraceutical Metabolism and Uses

[0049] Vitamins, cofactors, and nutraceuticals comprise another group of fine chemical molecules which higher animals have lost the ability to synthesize and so must ingest. These molecules are readily synthesized by other organisms, such as bacteria, fungi, algae and plants. These molecules are either bioactive substances themselves, or are precursors of biologically active substances which may serve as electron carriers or intermediates in a variety of metabolic pathways. Besides their nutritive value, these compounds also have significant industrial value as coloring agents, antioxidants, and catalysts or other processing aids. (For an overview of the structure, activity, and industrial applications of these compounds, see, for example, Ullman's Encyclopedia of Industrial Chemistry, “Vitamins” vol. A27, p. 443-613, VCH: Weinheim, 1996.) The term “vitamin” is art-recognized, and includes nutrients which are required by an organism for normal functioning, but which that organism cannot synthesize by itself. The group of vitamins may encompass cofactors and nutraceutical compounds. The language “cofactor” includes nonproteinaceous compounds required for a normal enzymatic activity to occur. Such compounds may be organic or inorganic; the cofactor molecules of the invention are preferably organic. The term “nutraceutical” includes dietary supplements having health benefits in plants and animals, particularly humans. Examples of such molecules are vitamins, antioxidants, and also certain lipids (e.g., polyunsaturated fatty acids).

[0050] The biosynthesis of these molecules in organisms capable of producing them, such as bacteria and plants, has been largely characterized (Friedrich, W. “Handbuch der Vitamine”, Urban und Schwarzenberg, 1987 ; Ullman's Encyclopedia of Industrial Chemistry, “Vitamins” vol. A27, p. 443-613, VCH: Weinheim, 1996; Michal, G. (1999) Biochemical Pathways: An Atlas of Biochemistry and Molecular Biology, John Wiley & Sons; Ong, A. S., Niki, E. & Packer, L. (1995) “Nutrition, Lipids, Health, and Disease” Proceedings of the UNESCO/Confederation of Scientific and Technological Associations in Malaysia, and the Society for Free Radical Research—Asia, held Sep. 1-3, 1994 at Penang, Malaysia, AOCS Press: Champaign, IL X, 374 S).

[0051] The metabolism and uses of certain of these vitamins are further explicated below.

[0052] Vitamin E

[0053] The fat-soluble vitamin E has received great attention for its essential role as an antioxidant in nutritional and clinical applications (Liebler D C 1993. Critical Reviews in Toxicology 23(2):147-169) thus representing a good area for food design, feed applications and pharmaceutical applications. In addition, beneficial effects are encountered in retarding diabetes-related high-age damages, anticancerogenic effects as well as a protective role against erythreme and skin aging. alpha-tocopherol as the most important antioxidans helps to prevent the oxidation of unsaturated fatty acids by oxygen in humans by its redox potential (Erin A N, Skrypin V V, Kragan V E 1985, Biochim. Biophy. Acta 815: 209).

[0054] The demand for this vitamin has increased year after year. The supply of tocopherols has been limited to the chemically synthesized racemate of alpha-tocopherol or a mixture of alpha-, beta(gamma)- and delta-tocopherols from vegetable oils. Altogether, the vitamin E group Dow comprises alpha-, beta-, gamma-, and delta-tocopherol as well as alpha-, beta-, gamma-, and delta-tocotrienol.

[0055] Biologically, tocopherols are indispensable components of the lipid bilayer of cell membranes. A reduction of availability of tocopheroles leads to structural and functional damaging of membranes. This stabilizing effect of the tocopherols on membranes is accepted to be related to three functions: 1) tocopherols react with lipid peroxide radicals, 2) quenching of reactive molecular oxygen, and 3) reducing the molecular mobility of the membrane bilayer by the formation of tocopherol-fatty acids complexes.

[0056] In addition to the occurrence of tocopherols in plants, their presence has been determined in various microorganisms, especially in many chlorophyll-containing organisms (Taketomi H, Soda K, Katsui G 1983, Vitamins (Japan) 57: 133-138). Algae, for example Euglenia gracilis, also contain tocopherols and Euglenia gracilis is described as a suitable host for the production of tocopherols since the most valuable form alpha-tocopherol is the major component of tocopherols (Shigeoka S, Onishi T, Nakano Y, Kitaoka S 1986, Agric. Biol. Chem. 50: 1063-1065). Also, yeasts and bacteria were found to synthesize tocopherols (Forbes M, Zilliken F, Roberts G, György P 1958, J. Am. Chem. Soc. 80: 385-389; Hughes and Tove 1982, J Bacteriol., 151: 1397-1402; Ruggeri B A, Gray R J H, Watkins T R, Tomlins R I 1985, Appl. Env. Microbiol. 50: 1404-1408).

[0057] Tocopherol is synthesized from geranlgeranylpyrophosphate which is generated from isopentenylpyrophosphate (IPP). IPP can be produced via two independent pathways. One pathway is located in the cytoplasm, whereas the other is located in the chloroplasts (for descriptions and reviews see Trelfall D R, Whistance G R in Aspects of Terpenoid Chemistry and Biochemistry, Goodwin T W Ed., Academic Press, London, 1971: 357-404; Michal G Ed. 1999, Biochemical Pathways, Spektrum Akademischer Verlag GmbH Heidelberg, and references cited therein; McCaskill D, Croteau R 1998, Tibtech 16: 349-355 and references cited therein; Rhomer M 1998, Progress in Drug Research 50: 135-154; Lichtenthaler H K 19998, Annu. Rev. Plant Physiol. Plant Mol. Biol. 50: 47-65; Lichtenthaler H K, Schwender J, Disch A, Rhomer M 1997, FEBS Letters 400: 271-274; Schultz G, Soil J 1980 Deutsche Tierärzthche Wochenschrift 87: 401-424; Arigoni D, Sagner S, Latzel C, Eisenreich W, Bacher A, Zenk, M H 1997 Proc. Natl. Acad. Sci. USA 94(2): 10600-10605). For a general review of isoprene biosynthesis and products derived from that pathway (Chappell 1995, Annu. Rev. Plant Physiol. Plant Mol. Biol. 46:521-547; Sharkey T D, 1996, Endeavor 20: 74-78).

[0058] The cyclic structures which are required for tocopherol biosynthesis are quinones. Quinones are synthesized from products of the shikimate pathway (for review see Dewick P M 1995, Natural Products Reports 12(6): 579-607; Weaver L M, Herrmann K M 1997, Trends in Plant Science 2(9): 346-351; Schmid J, Amrhein N 1995, Phytochemistry 39(4): 737-749).

[0059] Plant genes originating from Physcomitrella patens can be used to modify tocopherol metabolism in plants as well as algae and microorganisms enabling these host cells to increase their capacity to produce tocopherols as well as improving survival and fitness of the host cell.

[0060] Carotenoids

[0061] Carotenoids are naturally occurring pigments synthesized as hydrocarbons (carotenes) and their oxygenated derivatives (xantophylls) are produced by plants and microorganisms. The application potential was broadly investigated during the last 20 Years. Besides the use of carotenoids as coloring agents, it is assumed that carotenoids play an important role in the prevention of cancer (Rice-Evans et al. 1997, Free Radic. Res. 26:381-398; Gerster 1993, Int. J. Vitam. Nutr. Res. 63:93-121; Bendich 1993, Ann. New York Acad. Sci. 691:61-67) thus representing a good area for food design, feed applications and pharmaceutical applications.

[0062] The major function of carotenoids in plants and microoganisms is in protection against oxidative damage by quenching photosensensitizers interacting with singlet oxygen and scavenging peroxiradicals, thus preventing the accumulation of harmful oxygen species and subsequent maintenance of membrane integrity (Havaux 1998, Trends in Plant Science Vol 3 (4):147-151; Krinsky 1994, Pur Appl. Chem. 66:1003-1010). Thus an application is also given for the optimization of fermentation processes with respect to lesser susceptibility to oxidative damage. For a review of biotechnological potential see Sandmann et al. (1999, Tibtech 17; 233-237).

[0063] Plant genes originating from Physcomitrella patens can be used to modify carotenoid metabolism in plants as well as algae and microorganisms enabling these host cells to increase their capacity to produce carotenoids and to produce newly designed carotenoids as well as improving survival and fitness of the host cell due to the expression of plant acrotenoid biosynthetic genes.

[0064] Due to results obtained in labelling experiments it is clear that carotenes arise from the isoprenoid biosynthesis pathway via geranylgeranylpyrophosphate synthesis. For review of products of the isoprenoid biosynthetic pathway including carotenoids see Chappell 1995, Annu. Rev. Plant Physiol. Plant Mol. Biol. 46:521-547. The biosynthesis of carotenoids in microorganisms and plants is described in following articles and references therein: Armstrong 1997, Annu. Rev. Microbiol., 51:629-659; Sandman 1994, Eur. J. Biochem. 223:7-24; Misawa et al. 1995, J. Bacteriol. 177 (22):6575-6584; Hirschberg et al. 1997, Pure & Appl. Chem 69 (10):2151-2158; Lotan & Hirschberg 1995, FEBS Letters 364:125-128; U.S. Pat. No. 5,916,791).

[0065] Thiamin

[0066] The basic skeleton of thiamin contains a thiazole ring and a pyrimidine ring as described in Kegg-database (http://www.genome.ad.jp/kegg/dblinks/map/map00730.html). The exact chemical nomenclature is 3-((4-amino-2-methyl-pyrimidin-5-yl)methyl)-5-(2hydroxyethyl)4-methylthiazolium chloride.

[0067] Thiamine is widespread in nature, but occurs only in relatively small quantities (by example vegetables: 70 ug/100 g, potatoes: 170 ug/100 g, rice: 50-300 ug/100 g).

[0068] In plant products, free thiamin is the most abundant form. It is found in pericarp and the seeds of grains, cereal grains, dried vegetables, rice and potatoes. Oils, fats and highly processed foods such as refined sugars are essentially devoid of thiamin.

[0069] Although thiamin is widespread in foodstuffs, its concentration in individual foods varies widely and is relatively low since considerable amounts are destroyed on cooking, either by heat, the presence of metals, chlorine in the water or by reactive organic substances (Dong et al., J. Am. Diet. Assoc. 76, 1980, 156)

[0070] Thiamin serves a number of essential metabolic functions and its deficiency is associated with imbalances in carbohydrate status, with consequent deleterious effects on nerve functions. As a cofactor of enzymes in intermediate metabolism, thiamin pyrophosphate participates in the decarboxylation of alpha-keto acids and in the reversible a-ketol transfer reactions catalysed by transketolase in the pentose phasphate cycle (Krampitz in Thiamin Diphsphate and ist Catalytic Functions, Marcel Dekker, New York, 1970, Vilkas Vitamins Mécanismes d'Action Chimique, Ed Hermann, Paris 1994, p25).

[0071] Since extraction of thiamin from natural sources would not be economically profitable plant genes originating from Physcomitrella patens can be used to modify the thiamin metabolism in plants as well as algae and micro-organisms enabling these host cells to increase their capacity to produce thiamin as well as improving survival and fitness of the host cell.

[0072] Riboflavin

[0073] Riboflavin (vitamin B2) is synthesized from guanosine-5′-triphosphate (GTP) and ribulose-5′-phosphate in plants and microorganisms. The initial step is catalysed by the GTP cyclohydrolase II. Riboflavin is the precursor for flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) which besides NAD(P)H are the most important reducing äquivalents cellular anabolism. FMN and FAD comprise the prosthetic groups of several enzymes (flavoproteins, namely oxidases, dehydrogenases and oxidoreductases) and thus take part in more than 100 intracellular redox reactions.

[0074] Production of Riboflavin by fermentation is mainly performed with fungi like candida spec., Ashbya gossypii or Clostridium acetobutylicum and yields up to 7 g/l of the fine chemical, which is secreted to the medium. The fine chemical produced by ferentation is mainly used for feed purposes while chemical synthesis is performed for medical use. The fine chemical is quite stable against heat but very sensitive to illumination. Limited supply of riboflavin causes skin and growth diseases. Further the iron metabolism and lifetime of erithrocytes are perturbed probably due to a reduced activity of the flavoprotein gluthatione reductase. Riboflavin is found in many plants in concentrations about 0.5 mg/100 g. Cereals and fruits contain significantly lower amounts of the fine chemical. An increased production of riboflavine in plants such as cereals (preferably rice) and fruits is therefore appreciable.

[0075] Plant genes originating from Physcomitrella patens can be used to modify riboflavin metabolism in plants as well as algae and microorganisms enabling these host cells to increase their capacity to produce riboflavin as well as improving survival and fitness of the host cell.

[0076] Vitamin C

[0077] The main property of vitamin C (official IUPAC designation: L-ascorbic acid) is its strong reducing power due to ist endiol structure. Oxidation of the molecule proceeds in a two step process through semidehydroascorbic acid (a radical scavenger) to dehydroascorbic acid. The three forms of vitamin C establish a reversible redox system in living cells. Vitamin C is heat label and readily undergoes degradation under aerobic as well as anaerobic conditions in aquaeous solutions.

[0078] Vitamin C is ubiquitously found in higher eucaryotes and cyanobacteria. Plant leaves can accumulate as much as 10% of the carbohydrates as vitamin C. Plant fruits can contain even higher concentrations (e.g. more than 1% vitamin C of fresh weight in Malpigia glabra). Some plant species contain ascorbate in the bound forms ascorbigen (e.g. Brassica species) or eleaeocarpusin.

[0079] The biosynthesis of ascorbate is largely understood in animals algae and yeast (see Michal “Biochemical Pathways, p. 118f, Spektrum Verlag, 1999). For plants two alternative pathways have been discussed: The inversive pathway (via L-galactono-1,4-lactone) and the non inversive pathway (via D-glucosone and L-sorbosone) (for review see Loewus and Loewus CRC critical reviews in plant science 5, 101-119). Recent studies revealed that in higher plants L-galactono-1,4-lactone which is directly converted to ascorbate by the respective dehydrogenase is synthesized via mannose-1-phosphate, GDP-D-mannose, GDP-L-galactose, L-Galactose-1-phosphate and L-galactose (Wheeler and Smirnoff, Nature 393, p.365-368, 1998).

[0080] Besides glutathione ascorbate is the major antioxidant in plants. Ascorbate inactivates active oxygen and free radicals produced for example in photosynthesis and stress responses. The ascorbate peroxidase removes hydrogen peroxide. The oxidized forms of ascorbate monodehydroascorbate and dehydroascorbate are recycled by the respective reductases thereby maintaining a pool of reduced ascorbate. Monodehydroascorbate reductase utilizes NADH while dehydroascorbate reductase is linked to the glutathione cycle.

[0081] Vitamin C is part of several electron transport reactions linked e.g. to cytochrome P-450 hydroxylases. Further the enzyme 4-hydroxyphenylpyruvate dioxygenase involved in tyrosine degradation and in the biosynthesis of chinone compounds and tocopherols is depending on ascorbate.

[0082] Vitamine C deficiency causes scurvy, one of the oldest diseases in humankind due to the importance of ascorbate for the hydroxylation of prolines in structural proteins like collagen. The minimal daily dose preventing humans from the disease is about 50 mg/day. Streβ, alcohol and smoking lead to a higher demand for vitamin C. High doses can have beneficial effects against cold and cancer. A lack of vitamin C in old persons is linked to hyper cholesterinemia, arterosclerosis and anemia. The chemical synthesis of this fine chemical reached a volume of more than 6000 t/year.

[0083] Plant genes originating from Physcomitrella patens can be used to modify vitamin C metabolism in plants as well as algae and microorganisms enabling these host cells to increase their capacity to produce vitamin C as well as improving survival and fitness of the host cell.

[0084] Vitamin B6

[0085] The family of compounds collectively termed ‘vitamin B6’ (e.g., pyridoxine, pyridoxamine, pyridoxa-5′-phosphate, and the commercially used pyridoxin hydrochloride) are all derivatives of the common structural unit, 5-hydroxy-6-methylpyridine.

[0086] Vitamin B6 is produced by microorganisms and plants. In bacteria pyridoxine is synthesized from 1-deoxy-L-xylulose and 4-Hydroxythreonine, the later of which is produced by a series of reactions from erythrose 4-phosphate. A strong feedback regulation is probably underlying the biosynthesis in microorganisms which might explain why the maximum amounts of Vitamin B6 are still below 25 mg/L (produced from Pichia guilliermondi). Since the chemical synthesis of pyridoxin, the commercially most important form of Vitamin B6, is fairly easy, fermentation of B6 Vitamins has not yet been competitive.

[0087] The vitamin B6 biosynthesis in plants has not yet been investigated extensively. In plants vitamin B6 occurs mainly as pyridoxine of which a considerable part can occur in the glycosylated form as 5′O-(beta-glucopyranosyl)pyridoxine. This form is apparently well absorbed by animals but appears not to be entirely bioavailable. Thus shifting the vitamin B6 pool in plants to the pyridoxine form could be appreciable for food and feed applications.

[0088] Animals lack the ability to synthesize pyridoxin but they are able to interconvert it to the different forms of vitamin B6.

[0089] Pyridoxal phosphate is a cofactor essential to several enzymes mainly of the amino acid metabolism, which are most often involved in transamination, decarboxylation and racemisation reactions. Also phosphorylases involved in the carbohydrate metabolism are depending on pyridoxal phosphate. Modulation of vitamin B6 metabolism can thus have cross effects on multiple biosynthetic pathways.

[0090] A lack on vitamin B6 leads to neuronal distortions (neuritis), dermatitis and to an impairment of amino acid metablolism.

[0091] Plant genes originating from Physcomitrella patens can be used to modify vitamin B6 metabolism in plants as well as algae and microorganisms enabling these host cells to increase their capacity to produce vitamin B6 as well as improving survival and fitness of the host cell.

[0092] Pantothenate

[0093] Pantotenate (pantothenic acid, (R)-(+)-N-(2,4-dihydroxy-3,3-dimethyl-1-oxobutyl)-β-alanine) is the essential component of coenzyme A which is the mayor acyl-carrier in living cells. Coenzyme A is covalently linked to the acyl carrier protein (ACP) which is centrally involved in the biosynthesis of fatty acids. In nature pantothenate is rarely found in the free form but mainly as part of coenzyme A and ACP.

[0094] Pyruvate and Valin are the precursors for the biosynthesis of panthoic acid. The final steps in pantothenate biosynthesis consist of the ATP-driven condensation of β-alanine and pantoic acid. The enzymes responsible for the biosynthesis steps for the conversion to pantoic acid, to β-alanine and for the condensation to panthotenic acid are known. The metabolically active form of pantothenate is Coenzyme A, for which the biosynthesis proceeds in 5 enzymatic steps. Pantothenate, pyridoxal-5′-phosphate, cysteine and ATP are the precursors of Coenzyme A. These enzymes do not only catalyze the formation of panthothante, but also the production of (R)-pantoic acid, (R)-pantolacton, (R)-panthenol (provitamin B5), pantetheine (and its derivatives) and coenzyme A.

[0095] Pantothenate can be produced either by chemical synthesis or by fermentation. Pantothenate is being used mainly for feed applications. It further serves medical purposes as it promotes healing of skin injuries. The fine chemical is also used for protection from adverse effects of gamma irradiation during radiotherapy (Acta Oncologica 35, 1021-1026, 1996). The human daily demand for pantothenate is 4-10 mg and increases under streβ conditions. Alcohol deminishes the utilization of this fine chemical. The concentration of pantothenate in plants is usually lower than in animal tissues. An increased level of this vitamin in plants could therefore be appreciable.

[0096] Plant genes originating from Physcomitrella patens can be used to modify pantothenate biosynthesis in plants as well as algae and microorganisms enabling these host cells to increase their capacity to produce pantothenate as well as improving survival and fitness of the host cell.

[0097] Folate

[0098] The folates are a group of substances which all are derivatives of folic acid, which in turn is derived from L-glutamic acid, p-amino-benzoic acid and 6-methylpterin. The biosynthesis of folic acid and its derivatives, starting from the metabolism intermediates guanosine-5′-triphosphate (GTP), L-glutamic acid and p-amino-benzoic acid has been studied in detail in certain microorganisms.

[0099] Folic acid is synthesized de novo in plants and micro-organisms from the precursors GTP, p-amninobezoic acid and L-glutamic acid as described in the KEGG-database (http://www.genome.ad.jp/kegg/dblinks/map/map00730.html).

[0100] Mammals require Folic acid in their diet. Folates are present in all food products of plant origin, especially in green leafed vegetables. The folate content in ug/100 g of some foods its by example lettuce: 106-200, spinach: 78-194, asparagus: 50-195, cabbage: 30-79. Folate deficiency leads to impaired amino acid metabolism, protein synthesis and cell division.

[0101] Food processing, storage, and cooking reduce the content of folates considerably (Gregory, Adv. Food Nutr. Res. 33, 1989, 1-100). In particular oxidation results in inactive cleavage products. Folates can be stabilised for longer periods in the presence of reducing agents such as ascorbate.

[0102] Up to now is the extraction of folic acid from natural sources not economically viable. Thus plant genes originating from Physcomitrella patens can be used to modify the folic acid metabolism in plants as well as algae and microorganisms enabling these host cells to increase their capacity to produce folic acid as well as improving survival and fitness of the host cell.

[0103] Niacin

[0104] Niacin is one of the vitamins of the B complex. In accordance with the rules on nomenclature the institute of nutrition suggested that niacin be used as the generic name for both nicotinic and nicotinamide. Nicotinamide was shown to be a moiety of the coenzymes NAD (nicotinamide adenine dinucleotide) and NADP (nicotinamide adenine dinucleotide phosphate). These coenzymes are indispensable for many biochemical reactions in living cells. Nicotinic acid is the form present in food of plant origin, whereas nicotinamide occurs only in animal products. The biosynthetic pathway is described in the KEGG-database (http://www.genome.ad.jp/kegg/dblinks/map/mapOO760.html).

[0105] Niacin serves as precursor of two essential coenzymes: nicotinamide adenine dinucleotide and nicotinamide adenine dinucleotide phosphate. Both enzymes catalyse the metabolic transfer of hydrogen—one of the basic functions in the metabolism of proteins, fats and carbohydrates. This function is required for both the synthesis and the degradation of amino acids, fatty acids and carbohydrates. Another important task of the niacin coenzymes is their repeated intervention in the citric acid cycle. The citric acid cycle comprises many steps in which activated acetate is repeatedly oxidised and ATP is produced. Niacin thus plays an important part in the metabolic production and utilisation of energy.

[0106] Plant genes originating from Physcomitrella patens can be used to modify the niacin metabolism in plants as well as algae and microorganisms enabling these host cells to increase their capacity to produce niacin as well as improving survival and fitness of the host cell.

[0107] The large-scale production of the fine chemical compounds described above has largely relied on cell-free chemical syntheses, though some of these chemicals have also been produced by large-scale culture of microorganisms, such as riboflavin, Vitamin B6, pantothenate, and biotin. In vitro methodologies require significant inputs of materials and time, often at great cost. All though not yet applicable for large scale production it has been shown that production of fine chemicals can be enhanced in genetically modified plants as exemplified for phytoene in rice (Burkhardt et al. Plant Journal 11(5):1071-8, 1997) and vitamin E in Arabidopsis thaliana and other plants (Shintani nad DellaPenna. Science 282(5396):2098-100, 1998; WO99/23231).

[0108] Purine, Pyrimidine, Nucleoside and Nucleotide Metabolism and Uses

[0109] Purine and pyrimidine metabolism genes and their corresponding proteins are important targets for the therapy of tumor diseases and viral infections. The language “purine” or “pyrimidine” includes the nitrogenous bases which are constituents of nucleic acids, co-enzymes, and nucleotides. The term “nucleotide” includes the basic structural units of nucleic acid molecules. The language “nucleoside” includes molecules which serve as precursors to nucleotides, but which are lacking the phosphoric acid moiety that nucleotides possess. By inhibiting the biosynthesis of these molecules, or their mobilization to form nucleic acid molecules, it is possible to inhibit RNA and DNA synthesis; by inhibiting this activity in a fashion targeted to cancerous cells, the ability of tumor cells to divide and replicate may be inhibited. Additionally, there are nucleotides which do not form nucleic acid molecules, but rather serve as energy stores (i.e., ATP) or as coenzymes (i.e., FAD and NAD). In plants nucleotides are coupled to pentose and hexose sugars thereby activating these compounds for biosynthesis of carbohydrate polymers such as starch and cellulose.

[0110] However, purine and pyrimidine bases, nucleosides and nucleotides have other utilities: as intermediates in the biosynthesis of several fine chemicals (e.g., thiamine, S-adenosyl-methionine, folates, or riboflavin), as energy carriers for the cell (e.g., ATP or GTP), and for chemicals themselves, commonly used as flavor enhancers (e.g., IMP or GMP) or for several medicinal applications (see, for example, Kuninaka, A. (1996) Nucleotides and Related Compounds in Biotechnology vol. 6, Rehm et al., eds. VCH: Weinheim, p. 561-612).

[0111] Purine metabolism has been the subject of intensive research, and is essential to the normal functioning of the cell. The metabolism of these compounds has been characterized in detail in bacteria (for reviews see, for example, Zalkin, H. and Dixon, J. E. (1992) “de novo purine nucleotide biosynthesis”, in: Progress in Nucleic Acid Research and Molecular Biology, vol. 42, Academic Press:, p. 259-287; and Michal, G. (1999) “Nucleotides and Nucleosides”, Chapter 8 in: Biochemical Pathways: An Atlas of Biochemistry and Molecular Biology, Wiley: N.Y.).

[0112] In plants microorganisms and animals purine nucleotides are synthesized from phosphoribosyl pyrophosphate, in a series of steps through the intermediate compound inosine-5′-phosphate (IMP), resulting in the production of guanosine-5′-monophosphate (GMP) or adenosine-5′-monophosphate (AMP), from which the triphosphate forms utilized as nucleotides are readily formed. Pyrimidine biosynthesis proceeds by the formation of uridine-5′-monophosphate (UMP) from ribose-5-phosphate. UMP, in turn, is converted to cytidine-5′-triphosphate (CTP). The deoxy-forms of all nucleotides are produced in a one step reduction reaction from the diphosphate ribose form of the nucleotide to the diphosphate deoxyribose form of the nucleotide. Upon phosphorylation, these molecules are able to participate in DNA synthesis.

[0113] Impaired purine catabolism in higher animals can cause severe disease, such as gout. One utility for the modulation of nucleotides in plants is therefore to achieve an increased ratio of pyrimidines to purines in order to provide a diet suitable to cure this disease. This can be achieved by increasing the concentration of pyrimidine nucleotides or decreasing the concentration of purine nucleotides in edible plants.

[0114] Plant genes originating from Physcomitrella patens can be used to modify the nucleotide metabolism in plants as well as algae and microorganisms enabling these host cells to increase their capacity to produce nucleotides as well as improving survival and fitness of the host cell.

[0115] Another aspect of the invention pertains to the use of a produced fine chemical itself in the biosynthesis and production of other fine chemicals. For example, the produced fine chemical itself can have catalytical activity, thus supporting the conversion of one fine chemical into another fine chemical.

[0116] Elements and Methods of the Invention

[0117] The present invention is based, at least in part, on the discovery of novel molecules, referred to herein as MP nucleic acid and protein molecules, which play a role in or function in one or more cellular metabolic pathways in Physcomitrella patens. In one embodiment, the MP molecules catalyze an enzymatic reaction involving one or more amino acid, vitamin, cofactor, nutraceutical, nucleotide or nucleoside metabolic pathways. In a preferred embodiment, the activity of the MP molecules of the present invention in one or more Physcomitrella patens metabolic pathways for amino acids, vitamins, cofactors, nutraceuticals, nucleotides or nucleosides has an impact on the production of a desired fine chemical by this organism. In a particularly preferred embodiment, the MP proteins encoded by MP nucleotides of the invention are modulated in activity, such that the mircroorganisms' or plants' metabolic pathways which the MP proteins of the invention regulate are modulated in yield, production, and/or efficiency of production and/or transport of a desired fine chemical by microorganisms and plants.

[0118] The language, MP protein or MP polypeptide includes proteins which play a role in, e.g., catalyze an enzymatic reaction, in one or more amino acid, vitamin, cofactor, nutraceutical, nucleotide or nucleoside metabolic pathways in microorganisms and plants. Examples of MP proteins include those encoded by the MP genes set forth in Table 1 and Appendix A. The terms MP gene or MP nucleic acid sequence include nucleic acid sequences encoding an MP protein, which consist of a coding region and also corresponding untranslated 5′ and 3′ sequence regions. Examples of MP genes include those set forth in Table 1. The terms production or productivity are art-recognized and include the concentration of the fermentation product (for example, the desired fine chemical) formed within a given time and a given fermentation volume (e.g., kg product per hour per liter). The term efficiency of production includes the time required for a particular level of production to be achieved (for example, how long it takes for the cell to attain a particular rate of output of a fine chemical). The term yield or product/carbon yield is art-recognized and includes the efficiency of the conversion of the carbon source into the product (i.e., fine chemical). This is generally written as, for example, kg product per kg carbon source. By increasing the yield or production of the compound, the quantity of recovered molecules, or of useful recovered molecules of that compound in a given amount of culture over a given amount of time is increased. The terms biosynthesis or a biosynthetic pathway are art-recognized and include the synthesis of a compound, preferably an organic compound, by a cell from intermediate compounds in what may be a multistep and highly regulated process. The terms degradation or a degradation pathway are art-recognized and include the breakdown of a compound, preferably an organic compound, by a cell to degradation products (generally speaking, smaller or less complex molecules) in what may be a multistep and highly regulated process. The language metabolism is art-recognized and includes the totality of the biochemical reactions that take place in an organism. The metabolism of a particular compound, then, (e.g., the metabolism of amino acids, vitamins, cofactors, nucleotides and nucleosides) comprises the overall biosynthetic, modification, and degradation pathways in the cell related to this compound.

[0119] In another embodiment, the MP molecules of the invention are capable of modulating the production of a desired molecule, such as a fine chemical, in microorganisms and plants. There are a number of mechanisms by which the alteration of an MP protein of the invention may directly affect the yield, production, and/or efficiency of production of a fine chemical from a microorganisms or plant strain incorporating such an altered protein. Those MP proteins involved in the transport of fine chemical molecules within or from the cell may be increased in number or activity such that greater quantities of these compounds are transported across membranes. Similarly, those MP proteins involved in the import of nutrients necessary for the biosynthesis of one or more fine chemicals may be increased in number or activity such that these precursor, cofactor, or intermediate compounds are increased in concentration within a desired cell. Further MP proteins may be increased in number or activity which lead to a regeneration of a pool of fine chemicals in a desired state. The mutagenesis of one or more MP genes of the invention may also result in MP proteins having altered activities which indirectly impact the production of one or more desired fine chemicals from microorganisms, algae and plants. For example, a biosynthetic enzyme may be improved in efficiency, or its allosteric control region destroyed such that feedback inhibition of production of the compound is prevented. Similarly, a degradative enzyme may be deleted or modified by substitution, deletion, or addition such that its degradative activity is lessened for the desired compound without impairing the viability of the cell. In each case, the overall yield or rate of production of one of these desired fine chemicals may be increased.

[0120] It is also possible that such alterations in the protein and nucleotide molecules of the invention may improve the production of other fine chemicals besides the amino acids, vitamins, cofactors, nutraceuticals, nucleotides and nucleosides. Metabolism of any one compound is necessarily intertwined with other biosynthetic and degradative pathways within the cell, and necessary cofactors, intermediates, or substrates in one pathway are likely supplied or limited by another such pathway. Therefore, by modulating the activity of one or more of the proteins of the invention, the production or efficiency of activity of another fine chemical biosynthetic or degradative pathway may be impacted. For example, amino acids serve as the structural units of all proteins, yet may be present intracellularly in levels which are limiting for protein synthesis; therefore, by increasing the efficiency of production or the yields of one or more amino acids within the cell, proteins, such as biosynthetic or degradative proteins, may be more readily synthesized. Likewise, an alteration in a metabolic pathway enzyme such that a particular side reaction becomes more or less favored may result in the over- or under-production of one or more compounds which are utilized as intermediates or substrates for the production of a desired fine chemical.

[0121] MP proteins of the invention involved in the export of waste products may be increased in number or activity such that the normal metabolic wastes of the cell (possibly increased in quantity due to the overproduction of the desired fine chemical) are efficiently exported before they are able to damage nucleotides and proteins within the cell (which would decrease the viability of the cell) or to interfere with fine chemical biosynthetic pathways (which would decrease the yield, production, or efficiency of production of the desired fine chemical). Further, the relatively large intracellular quantities of the desired fine chemical may in itself be toxic to the cell, so by increasing the activity or number of transporters able to export this compound from the cell, one may increase the viability of the cell in culture, in turn leading to a greater number of cells in the culture producing the desired fine chemical.

[0122] The MP proteins of the invention may also be manipulated such that the relative amounts of different amino acids, vitamins, cofactors, nutraceuticals, nucleotides or nucleosides are produced. The isolated nucleic acid sequences of the invention are contained within the genome of a Physcomitrella patens strain available through the moss collection of the University of Hamburg. The nucleotide sequence of the isolated Physcomitrella patens MP cDNAs and the predicted amino acid sequences of the respective Physcomitrella patens MP proteins are shown in Appendices A and B, respectively.

[0123] The present invention also pertains to proteins which have an amino acid sequence which is substantially homologous to an amino acid sequence of Appendix B. As used herein, a protein which has an amino acid sequence which is substantially homologous to a selected amino acid sequence is least about 50% homologous to the selected amino acid sequence, e.g., the entire selected amino acid sequence. A protein which has an amino acid sequence which is substantially homologous to a selected amino acid sequence can also be least about 50-60%, preferably at least about 60-70%, and more preferably at least about 70-80%, 80-90%, or 90-95%, and most preferably at least about 96%, 97%, 98%, 99% or more homologous to the selected amino acid sequence.

[0124] The MP protein or a biologically active portion or fragment thereof of the invention can catalyze an enzymatic reaction in one or more amino acid, vitamin, cofactor, nutraceutical, nucleotide, or nucleoside metabolic pathways in plants and microorganisms, or have one or more of the activities set forth in Table 1. Various aspects of the invention are described in further detail in the following subsections:

[0125] A. Isolated Nucleic Acid Molecules

[0126] One aspect of the invention pertains to isolated nucleic acid molecules that encode MP polypeptides or biologically active portions thereof, as well as nucleic acid fragments sufficient for use as hybridization probes or primers for the identification or amplification of MP protein-encoding nucleic acid (e.g., MP DNA). As used herein, the term “nucleic acid molecule” is intended to include DNA molecules (e.g., cDNA or genomic DNA) and RNA molecules (e.g., mRNA) and analogs of the DNA or RNA generated using nucleotide analogs. This term also encompasses untranslated sequence located at both the 3′ and 5′ ends of the coding region of the gene: at least about 100 nucleotides of sequence upstream from the 5′ end of the coding region and at least about 20 nucleotides of sequence downstream from the 3′ end of the coding region of the gene. The nucleic acid molecule can be single-stranded or double-stranded, but preferably is double-stranded DNA. An “isolated” nucleic acid molecule is one which is separated from other nucleic acid molecules which are present in the natural source of the nucleic acid. Preferably, an “isolated” nucleic acid is free of sequences which naturally flank the nucleic acid (i.e., sequences located at the 5′ and 3′ ends of the nucleic acid) in the genomic DNA of the organism from which the nucleic acid is derived. For example, in various embodiments, the isolated MP nucleic acid molecule can contain less than about 5 kb, 4 kb, 3 kb, 2 kb, 1 kb, 0.5 kb or 0.1 kb of nucleotide sequences which naturally flank the nucleic acid molecule in genomic DNA of the cell from which the nucleic acid is derived (e.g, a Physcomitrella patens cell). Moreover, an “isolated” nucleic acid molecule, such as a cDNA molecule, can be substantially free of other cellular material, or culture medium when produced by recombinant techniques, or chemical precursors or other chemicals when chemically synthesized.

[0127] A nucleic acid molecule of the present invention, e.g., a nucleic acid molecule having a nucleotide sequence of Appendix A, or a portion thereof, can be isolated using standard molecular biology techniques and the sequence information provided herein. For example, a P. patens MP cDNA can be isolated from a P. patens library using all or portion of one of the sequences of Appendix A as a hybridization probe and standard hybridization techniques (e.g., as described in Sambrook et al., Molecular Cloning: A Laboratory Manual. 2nd, ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989). Moreover, a nucleic acid molecule encompassing all or a portion of one of the sequences of Appendix A can be isolated by the polymerase chain reaction using oligonucleotide primers designed based upon this sequence (e.g., a nucleic acid molecule encompassing all or a portion of one of the sequences of Appendix A can be isolated by the polymerase chain reaction using oligonucleotide primers designed based upon this same sequence of Appendix A). For example, mRNA can be isolated from plant cells (e.g., by the guanidinium-thiocyanate extraction procedure of Chirgwin et al. (1979) Biochemistry 18: 5294-5299) and cDNA can be prepared using reverse transcriptase (e.g., Moloney MLV reverse transcriptase, available from Gibco/BRL, Bethesda, Md.; or AMV reverse transcriptase, available from Seikagaku America, Inc., St. Petersburg, Fla.). Synthetic oligonucleotide primers for polymerase chain reaction amplification can be designed based upon one of the nucleotide sequences shown in Appendix A. A nucleic acid of the invention can be amplified using cDNA or, alternatively, genomic DNA, as a template and appropriate oligonucleotide primers according to standard PCR amplification techniques. The nucleic acid so amplified can be cloned into an appropriate vector and characterized by DNA sequence analysis. Furthermore, oligonucleotides corresponding to an MP nucleotide sequence can be prepared by standard synthetic techniques, e.g., using an automated DNA synthesizer.

[0128] In a preferred embodiment, an isolated nucleic acid molecule of the invention comprises one of the nucleotide sequences shown in Appendix A. The sequences of Appendix A correspond to the Physcomitrella patens MP cDNAs of the invention. This cDNA comprises sequences encoding MP proteins (i.e., the “coding region”, indicated in each sequence in Appendix A), as well as 5′ untranslated sequences and 3′ untranslated sequences. Alternatively, the nucleic acid molecule can comprise only the coding region of any of the sequences in Appendix A or can contain whole genomic fragments isolated from genomic DNA.

[0129] For the purposes of this application, it will be understood that each of the sequences set forth in Appendix A has an identifying entry number Each of these sequences comprises up to three parts: a 5′ upstream region, a coding region, and a downstream region. Each of these three regions is identified by the same entry number designation to eliminate confusion. The recitation one of the sequences in Appendix A, then, refers to any of the sequences in Appendix A, which may be distinguished by their differing entry number designations. The coding region of each of these sequences is translated into a corresponding amino acid sequence, which is set forth in Appendix B. The sequences of Appendix B are identified by the same entry numbers designations as Appendix A, such that they can be readily correlated. For example, the amino acid sequence in Appendix B designated 87_ck17_g05fwd is a translation of the coding region of the nucleotide sequence of nucleic acid molecule 87_ck17_g05fwd in Appendix A, and the amino acid sequence in Appendix B designated 42_pprot1 is a translation of the coding region of the nucleotide sequence of nucleic acid molecule 42_pprot1 in Appendix A.

[0130] In another preferred embodiment, an isolated nucleic acid molecule of the invention comprises a nucleic acid molecule which is a complement of one of the nucleotide sequences shown in Appendix A, or a portion thereof. A nucleic acid molecule which is complementary to one of the nucleotide sequences shown in Appendix A is one which is sufficiently complementary to one of the nucleotide sequences shown in Appendix A such that it can hybridize to one of the nucleotide sequences shown in Appendix A, thereby forming a stable duplex.

[0131] In still another preferred embodiment, an isolated nucleic acid molecule of the invention comprises a nucleotide sequence which is at least about 50-60%, preferably at least about 60-70%, more preferably at least about 70-80%, 80-90%, or 90-95%, and even more preferably at least about 95%, 96%, 97%, 98%, 99% or more homologous to a nucleotide sequence shown in Appendix A, or a portion thereof. In an additional preferred embodiment, an isolated nucleic acid molecule of the invention comprises a nucleotide sequence which hybridizes, e.g., hybridizes under stringent conditions, to one of the nucleotide sequences shown in Appendix A, or a portion thereof.

[0132] Moreover, the nucleic acid molecule of the invention can comprise only a portion of the coding region of one of the sequences in Appendix A, for example a fragment which can be used as a probe or primer or a fragment encoding a biologically active portion of an MP protein. The nucleotide sequences determined from the cloning of the MP genes from P. patens allows for the generation of probes and primers designed for use in identifying and/or cloning MP proteinhomologues in other cell types and organisms, as well as MP protein homologues from other mosses or related species. The probe/primer typically comprises substantially purified oligonucleotide. The oligonucleotide typically comprises a region of nucleotide sequence that hybridizes under stringent conditions to at least about 12, preferably about 25, more preferably about 40, 50 or 75 consecutive nucleotides of a sense strand of one of the sequences set forth in Appendix A, an anti-sense sequence of one of the sequences set forth in Appendix A, or naturally occurring mutants thereof. Primers based on a nucleotide sequence of Appendix A can be used in PCR reactions to clone MP protein homologues. Probes based on the MP nucleotide sequences can be used to detect transcripts or genomic sequences encoding the same or homologous proteins. In preferred embodiments, the probe further comprises a label group attached thereto, e.g. the label group can be a radioisotope, a fluorescent compound, an enzyme, or an enzyme cofactor. Such probes can be used as a part of a genomic marker test kit for identifying cells which misexpress an MP protein, such as by measuring a level of an MP protein-encoding nucleic acid in a sample of cells, e.g., detecting MP mRNA levels or determining whether a genomic MPgene has been mutated or deleted.

[0133] In one embodiment, the nucleic acid molecule of the invention encodes a protein or portion thereof which includes an amino acid sequence which is sufficiently homologous to an amino acid sequence of Appendix B such that the protein or portion thereof maintains the ability to catalyze an enzymatic reaction in an amino acid, vitamin, cofactor, nutraceutical, nucleotide or nucleoside metabolic pathway in microorganisms or plants. As used herein, the language “sufficiently homologous” refers to proteins or portions thereof which have amino acid sequences which include a minimum number of identical or equivalent (e.g., an amino acid residue which has a similar side chain as an amino acid residue in one of the sequences of Appendix B) amino acid residues to an amino acid sequence of Appendix B such that the protein or portion thereof is able to catalyze an enzymatic reaction in an amino acid, vitamin, cofactor, nutraceutical, nucleotide or nucleoside metabolic pathway in microorganisms or plants. Protein members of such metabolic pathways, as described herein, function to catalyze the biosynthesis or degradation or stabilisation of one or more of: amino acids, vitamins, cofactors, nutraceuticals, nucleotides or nucleosides. Examples of such activities are also described herein. Thus, the function of an MP protein” contributes either directly or indirectly to the yield, production, and/or efficiency of production of one or more fine chemicals. Examples of MP protein activities are set forth in Table 1.

[0134] In another embodiment, the protein is at least about 50-60%, preferably at least about 60-70%, and more preferably at least about 70-80%, 80-90%, 90-95%, and most preferably at least about 96%, 97%, 98%, 99% or more homologous to an entire amino acid sequence of Appendix B.

[0135] Portions of proteins encoded by the MP nucleic acid molecules of the invention are preferably biologically active portions of one of the MP protein. As used herein, the term “biologically active portion of an MP protein” is intended to include a portion, e.g., a domain/motif, of an MP protein that participates in the metabolism of fine chemicals like amino acids, vitamins, cofactors, nutraceuticals, nucleotides, or nucleosides in microorganisms or plants or has an activity as set forth in Table 1. To determine whether an MP protein or a biologically active portion thereof can participate in the metabolism of fine chemicals like amino acids, vitamins, cofactors, nutraceuticals, nucleotides, or nucleosides in microorganisms or plants, an assay of enzymatic activity may be performed. Such assay methods are well known to those skilled in the art, as detailed in Example 17 of the Exemplification.

[0136] Additional nucleic acid fragments encoding biologically active portions of an MP protein can be prepared by isolating a portion of one of the sequences in Appendix B, expressing the encoded portion of the MP protein or peptide (e.g., by recombinant expression in vitro) and assessing the activity of the encoded portion of the MP protein or peptide.

[0137] The invention further encompasses nucleic acid molecules that differ from one of the nucleotide sequences shown in Appendix A (and portions thereof) due to degeneracy of the genetic code and thus encode the same MP protein as that encoded by the nucleotide sequences shown in Appendix A. In another embodiment, an isolated nucleic acid molecule of the invention has a nucleotide sequence encoding a protein having an amino acid sequence shown in Appendix B. In a still further embodiment, the nucleic acid molecule of the invention encodes a full length Physcomitrella patens protein which is substantially homologous to an amino acid sequence of Appendix B (encoded by an open reading frame shown in Appendix A).

[0138] In addition to the Physcomitrella patens MP nucleotide sequences shown in Appendix A, it will be appreciated by those skilled in the art that DNA sequence polymorphisms that lead to changes in the amino acid sequences of MP proteins may exist within a population (e.g., the Physcomitrella patens population). Such genetic polymorphism in the MP gene may exist among individuals within a population due to natural variation. As used herein, the terms “gene” and “recombinant gene” refer to nucleic acid molecules comprising an open reading frame encoding an MP protein, preferably a Physcomitrella patens MP protein. Such natural variations can typically result in 1-5% variance in the nucleotide sequence of the MP gene. Any and all such nucleotide variations and resulting amino acid polymorphisms in MP proteins that are the result of natural variation and that do not alter the functional activity of MP proteins are intended to be within the scope of the invention.

[0139] Nucleic acid molecules corresponding to natural variants and non-Physcomitrella patens homologues of the Physcomitrella patens MP cDNA of the invention can be isolated based on their homology to Physcomitrella patens MP nucleic acid disclosed herein using the Physcomitrella patens cDNA, or a portion thereof, as a hybridization probe according to standard hybridization techniques under stringent hybridization conditions. Accordingly, in another embodiment, an isolated nucleic acid molecule of the invention is at least 15 nucleotides in length and hybridizes under stringent conditions to the nucleic acid molecule comprising a nucleotide sequence of Appendix A. In other embodiments, the nucleic acid is at least 30, 50, 100, 250 or more nucleotides in length. As used herein, the term “hybridizes under stringent conditions” is intended to describe conditions for hybridization and washing under which nucleotide sequences at least 60% homologous to each other typically remain hybridized to each other. Preferably, the conditions are such that sequences at least about 65%, more preferably at least about 70%, and even more preferably at least about 75% or more homologous to each other typically remain hybridized to each other. Such stringent conditions are known to those skilled in the art and can be found in Current Protocols in Molecular Biology, John Wiley & Sons, N.Y. (1989), 6.3.1-6.3.6. A preferred, non-limiting example of stringent hybridization conditions are hybridization in 6×sodium chloride/sodium citrate (SSC) at about 45° C., followed by one or more washes in 0.2×SSC, 0.1% SDS at 50-65° C. Preferably, an isolated nucleic acid molecule of the invention that hybridizes under stringent conditions to a sequence of Appendix A corresponds to a naturally-occurring nucleic acid molecule. As used herein, a “naturally-occurring” nucleic acid molecule refers to an RNA or DNA molecule having a nucleotide sequence that occurs in nature (e.g., encodes a natural protein). In one embodiment, the nucleic acid encodes a natural Physcomitrella patens MP protein.

[0140] In addition to naturally-occurring variants of the MP proteinsequence that may exist in the population, the skilled artisan will further appreciate that changes can be introduced by mutation into a nucleotide sequence of Appendix A, thereby leading to changes in the amino acid sequence of the encoded MP protein, without altering the functional ability of the MP protein. For example, nucleotide substitutions leading to amino acid substitutions at “non-essential” amino acid residues can be made in a sequence of Appendix A. A “non-essential” amino acid residue is a residue that can be altered from the wild-type sequence of one of the MP proteins (Appendix B) without altering the activity of said MP protein, whereas an essential amino acid residue is required for MP protein activity. Other amino acid residues, however, (e.g., those that are not conserved or only semi-conserved in the domain having MP protein activity) may not be essential for activity and thus are likely to be amenable to alteration without altering MP protein activity.

[0141] Accordingly, another aspect of the invention pertains to nucleic acid molecules encoding MP proteins that contain changes in amino acid residues that are not essential for MP protein activity. Such MP proteins differ in amino acid sequence from a sequence contained in Appendix B yet retain at least one of the MP protein activities described herein. In one embodiment, the isolated nucleic acid molecule comprises a nucleotide sequence encoding a protein, wherein the protein comprises an amino acid sequence at least about 50% homologous to an amino acid sequence of Appendix B and is able to catalyze an enzymatic reaction in an amino acid, vitamin, cofactor, nutraceutical, nucleotide or nucleoside metabolic pathway in P. patens, or has one or more activities set forth in Table 1. Preferably, the protein encoded by the nucleic acid molecule is at least about 50-60% homologous to one of the sequences in Appendix B, more preferably at least about 60-70% homologous to one of the sequences in Appendix B, even more preferably at least about 70-80%, 80-90%, 90-95% homologous to one of the sequences in Appendix B, and most preferably at least about 96%, 97%, 98%, or 99% homologous to one of the sequences in Appendix B.

[0142] To determine the percent homology of two amino acid sequences (e.g., one of the sequences of Appendix B and a mutant form thereof) or of two nucleic acids, the sequences are aligned for optimal comparison purposes (e.g., gaps can be introduced in the sequence of one protein or nucleic acid for optimal alignment with the other protein or nucleic acid). The amino acid residues or nucleotides at corresponding amino acid positions or nucleotide positions are then compared. When a position in one sequence (e.g., one of the sequences of Appendix B) is occupied by the same amino acid residue or nucleotide as the corresponding position in the other sequence (e.g., a mutant form of the sequence selected from Appendix B), then the molecules are homologous at that position (i.e., as used herein amino acid or nucleic acid “homology” is equivalent to amino acid or nucleic acid “identity”). The percent homology between the two sequences is a function of the number of identical positions shared by the sequences (i.e., % homology=numbers of identical positions/total numbers of positions×100).

[0143] An isolated nucleic acid molecule encoding an MP protein homologous to a protein sequence of Appendix B can be created by introducing one or more nucleotide substitutions, additions or deletions into a nucleotide sequence of Appendix A such that one or more amino acid substitutions, additions or deletions are introduced into the encoded protein. Mutations can be introduced into one of the sequences of Appendix A by standard techniques, such as site-directed mutagenesis and PCR-mediated mutagenesis. Preferably, conservative amino acid substitutions are made at one or more predicted non-essential amino acid residues. A “conservative amino acid substitution” is one in which the amino acid residue is replaced with an amino acid residue having a similar side chain. Families of amino acid residues having similar side chains have been defined in the art. These families include amino acids with basic side chains (e.g., lysine, arginine, histidine), acidic side chains (e.g., aspartic acid, glutamic acid), uncharged polar side chains (e.g., glycine, asparagine, glutamine, serine, threonine, tyrosine, cysteine), nonpolar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan), beta-branched side chains (e.g., threonine, valine, isoleucine) and aromatic side chains (e.g., tyrosine, phenylalanine, tryptophan, histidine). Thus, a predicted nonessential amino acid residue in an MP protein is preferably replaced with another amino acid residue from the same side chain family. Alternatively, in another embodiment, mutations can be introduced randomly along all or part of an MP protein coding sequence, such as by saturation mutagenesis, and the resultant mutants can be screened for an MP protein activity described herein to identify mutants that retain MP protein activity. Following mutagenesis of one of the sequences of Appendix A, the encoded protein can be expressed recombinantly and the activity of the protein can be determined using, for example, assays described herein (see Example 17 of the Exemplification).

[0144] In addition to the nucleic acid molecules encoding MP proteins described above, another aspect of the invention pertains to isolated nucleic acid molecules which are antisense thereto. An “antisense” nucleic acid comprises a nucleotide sequence which is complementary to a “sense” nucleic acid encoding a protein, e.g., complementary to the coding strand of a double-stranded cDNA molecule or complementary to an mRNA sequence. Accordingly, an antisense nucleic acid can hydrogen bond to a sense nucleic acid. The antisense nucleic acid can be complementary to an entire MP cDNA coding strand, or to only a portion thereof. In one embodiment, an antisense nucleic acid molecule is antisense to a “coding region” of the coding strand of a nucleotide sequence encoding an MP protein. The term “coding region” refers to the region of the nucleotide sequence comprising codons which are translated into amino acid residues. In another embodiment, the antisense nucleic acid molecule is antisense to a “noncoding region” of the coding strand of a nucleotide sequence encoding MP proteins. The term “noncoding region” refers to 5′ and 3′ sequences which flank the coding region that are not translated into amino acids (i.e., also referred to as 5′ and 3′ untranslated regions).

[0145] Given the coding strand sequences encoding MP proteins disclosed herein (e.g., the sequences set forth in Appendix A), antisense nucleic acids of the invention can be designed according to the rules of Watson and Crick base pairing. The antisense nucleic acid molecule can be complementary to the entire coding region of MP mRNA, but more preferably is an oligonucleotide which is antisense to only a portion of the coding or noncoding region of MP mRNA. For example, the antisense oligonucleotide can be complementary to the region surrounding the translation start site of MP mRNA. An antisense oligonucleotide can be, for example, about 5, 10, 15, 20, 25, 30, 35, 40, 45 or 50 nucleotides in length. An antisense nucleic acid of the invention can be constructed using chemical synthesis and enzymatic ligation reactions using procedures known in the art. For example, an antisense nucleic acid (e.g., an antisense oligonucleotide) can be chemically synthesized using naturally occurring nucleotides or variously modified nucleotides designed to increase the biological stability of the molecules or to increase the physical stability of the duplex formed between the antisense and sense nucleic acids, e.g., phosphorothioate derivatives and acridine substituted nucleotides can be used. Examples of modified nucleotides which can be used to generate the antisense nucleic acid include 5-fluorouracil, 5-bromouracil, 5-chlorouracil, 5-iodouracil, hypoxanthine, xanthine, 4-acetylcytosine, 5-(carboxyhydroxylmethyl)uracil, 5-carboxymethylaminomethyl-2-thiouridine, 5-carboxymethylaminomethyluracil, dihydrouracil, beta-D-galactosylqueosine, inosine, N6-isopentenyladenine, 1-methylguanine, 1-methylinosine, 2,2-dimethylguanine, 2-methyladenine, 2-methylguanine, 3-methylcytosine, 5-methylcytosine, N6-adenine, 7-methylguanine, 5-methylaminomethyluracil, 5-methoxyaminomethyl-2-thiouracil, beta-D-mannosylqueosine, 5′-methoxycarboxymethyluracil, 5-methoxyuracil, 2-methylthio-N6-isopentenyladenine, uracil-5-oxyacetic acid(v), wybutoxosine, pseudouracil, queosine, 2-thiocytosine, 5-methyl-2-thiouracil, 2-thiouracil, 4-thiouracil, 5-methyluracil, uracil-5-oxyacetic acid methylester, uracil-5-oxyacetic acid(v), 5-methyl-2-thiouracil, 3-(3-amino-3-N-2-carboxypropyl)uracil, (acp3)w, and 2,6-diaminopurine. Alternatively, the antisense nucleic acid can be produced biologically using an expression vector into which a nucleic acid has been subcloned in an antisense orientation (i.e., RNA transcribed from the inserted nucleic acid will be of an antisense orientation to a target nucleic acid of interest, described further in the following subsection).

[0146] The antisense nucleic acid molecules of the invention are typically administered to a cell or generated in situ such that they hybridize with or bind to cellular mRNA and/or genomic DNA encoding an MP protein to thereby inhibit expression of the protein, e.g., by inhibiting transcription and/or translation. The hybridization can be by conventional nucleotide complementarity to form a stable duplex, or, for example, in the case of an antisense nucleic acid molecule which binds to DNA duplexes, through specific interactions in the major groove of the double helix. The antisense molecule can be modified such that it specifically binds to a receptor or an antigen expressed on a selected cell surface, e.g., by linking the antisense nucleic acid molecule to a peptide or an antibody which binds to a cell surface receptor or antigen. The antisense nucleic acid molecule can also be delivered to cells using the vectors described herein. To achieve sufficient intracellular concentrations of the antisense molecules, vector constructs in which the antisense nucleic acid molecule is placed under the control of a strong prokaryotic, viral, or eukaryotic including plant promoters are preferred.

[0147] In yet another embodiment, the antisense nucleic acid molecule of the invention is an α-anomeric nucleic acid molecule. An α-anomeric nucleic acid molecule forms specific double-stranded hybrids with complementary RNA in which, contrary to the usual β-units, the strands run parallel to each other (Gaultier et al. (1987) Nucleic Acids. Res. 15:6625-6641). The antisense nucleic acid molecule can also comprise a 2′-o-methylribonucleotide (Inoue et al. (1987) Nucleic Acids Res. 15:6131-6148) or a chimeric RNA-DNA analogue (Inoue et al. (1987) FEBS Lett. 215:327-330).

[0148] In still another embodiment, an antisense nucleic acid of the invention is a ribozyme. Ribozymes are catalytic RNA molecules with ribonuclease activity which are capable of cleaving a single-stranded nucleic acid, such as an mRNA, to which they have a complementary region. Thus, ribozymes (e.g., hammerhead ribozymes (described in Haselhoff and Gerlach (1988) Nature 334:585-591)) can be used to catalytically cleave MP mRNA transcripts to thereby inhibit translation of MP mRNA. A ribozyme having specificity for an MP protein-encoding nucleic acid can be designed based upon the nucleotide sequence of an MP protein cDNA disclosed herein. For example, a derivative of a Tetrahymena L-19 IVS RNA can be constructed in which the nucleotide sequence of the active site is complementary to the nucleotide sequence to be cleaved in an MP protein-encoding mRNA. See, e.g., Cech et al. U.S. Pat. Nos. 4,987,071 and 5,116,742. Alternatively, MP mRNA can be used to select a catalytic RNA having a specific ribonuclease activity from a pool of RNA molecules. See, e.g., Bartel, D. and Szostak, J. W. (1993) Science 261:1411-1418.

[0149] Alternatively, MP gene expression can be inhibited by targeting nucleotide sequences complementary to the regulatory region of an MP nucleotide sequence (e.g., an MP promoter and/or enhancers) to form triple helical structures that prevent transcription of an MP gene in target cells. See generally, Helene, C. (1991) Anticancer Drug Des. 6(6):569-84; Helene, C. et al. (1992) Ann. NY. Acad. Sci. 660:27-36; and Maher, L. J. (1992) Bioassays 14(12):807-15.

[0150] B. Recombinant Expression Vectors and Host Cells

[0151] Another aspect of the invention pertains to vectors, preferably expression vectors, containing a nucleic acid encoding an MP protein (or a portion thereof). As used herein, the term “vector” refers to a nucleic acid molecule capable of transporting another nucleic acid to which it has been linked. One type of vector is a “plasmid”, which refers to a circular double stranded DNA loop into which additional DNA segments can be ligated. Another type of vector is a viral vector, wherein additional DNA segments can be ligated into the viral genome. Certain vectors are capable of autonomous replication in a host cell into which they are introduced (e.g., bacterial vectors having a bacterial origin of replication and episomal mammalian vectors). Other vectors (e.g., non-episomal mammalian vectors) are integrated into the genome of a host cell upon introduction into the host cell, and thereby are replicated along with the host genome. Moreover, certain vectors are capable of directing the expression of genes to which they are operatively linked. Such vectors are referred to herein as “expression vectors”. In general, expression vectors of utility in recombinant DNA techniques are often in the form of plasmids. In the present specification, “plasmid” and “vector” can be used interchangeably as the plasmid is the most commonly used form of vector. However, the invention is intended to include such other forms of expression vectors, such as viral vectors (e.g., replication defective retroviruses, adenoviruses and adeno-associated viruses), which serve equivalent functions.

[0152] The recombinant expression vectors of the invention comprise a nucleic acid of the invention in a form suitable for expression of the nucleic acid in a host cell, which means that the recombinant expression vectors include one or more regulatory sequences, selected on the basis of the host cells to be used for expression, which is operatively linked to the nucleic acid sequence to be expressed. Within a recombinant expression vector, “operably linked” is intended to mean that the nucleotide sequence of interest is linked to the regulatory sequence(s) in a manner which allows for expression of the nucleotide sequence are fused to each other so that both sequences fulfill the proposed function addicted to the sequence used. (e.g., in an in vitro transcription/translation system or in a host cell when the vector is introduced into the host cell). The term “regulatory sequence” is intended to include promoters, enhancers and other expression control elements (e.g., polyadenylation signals). Such regulatory sequences are described, for example, in Goeddel; Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990) or in Gruber and Crosby, in: Methods in Plant Molecular Biology and Biotechnolgy, CRC Press, Boca Raton, Fla., eds.: Glick and Thompson, Chapter 7, 89-108 including the references therein. Regulatory sequences include those which direct constitutive expression of a nucleotide sequence in many types of host cell and those which direct expression of the nucleotide sequence only in certain host cells or under certain conditions. It will be appreciated by those skilled in the art that the design of the expression vector can depend on such factors as the choice of the host cell to be transformed, the level of expression of protein desired, etc. The expression vectors of the invention can be introduced into host cells to thereby produce proteins or peptides, including fusion proteins or peptides, encoded by nucleic acids as described herein (e.g., MP proteins, mutant forms of MP proteins, fusion proteins, etc.).

[0153] The recombinant expression vectors of the invention can be designed for expression of MP proteins in prokaryotic or eukaryotic cells. For example, MP genes can be expressed in bacterial cells such as C. glutamicum, insect cells (using baculovirus expression vectors), yeast and other fungal cells (see Romanos, M. A. et al. (1992) Foreign gene expression in yeast: a review, Yeast 8: 423-488; van den Hondel, C. A. M. J. J. et al. (1991) Heterologous gene expression in filamentous fungi, in: More Gene Manipulations in Fungi, J. W. Bennet & L. L. Lasure, eds., p. 396-428: Academic Press: San Diego; and van den Hondel, C. A. M. J. J. & Punt, P. J. (1991) Gene transfer systems and vector development for filamentous fungi, in: Applied Molecular Genetics of Fungi, Peberdy, J. F. et al., eds., p. 1-28, Cambridge University Press: Cambridge), algae (Falciatore et al., 1999, Marine Biotechnology.1 (3):239-251), ciliates of the types: Holotrichia, Peritrichia, Spirotrichia, Suctoria, Tetrahymena, Paramecium, Colpidium, Glaucoma, Platyophrya, Potomacus, Pseudocohnilembus, Euplotes, Engelmaniella, and Stylonychia, especially of the genus Stylonychia lemnae with vectors following a transformation method as described in WO9801572 and multicellular plant cells (see Schmidt, R. and Willmitzer, L. (1988), High efficiency Agrobacterium tumefaciens-mediated transformation of Arabidopsis thaliana leaf and cotyledon explants, Plant Cell Rep.: 583-586); Plant Molecular Biology and Biotechnology, C Press, Boca Raton, Fla., chapter 6/7, S.71-119 (1993); F. F. White, B. Jenes et al., Techniques for Gene Transfer, in: Transgenic Plants, Vol. 1, Engineering and Utilization, eds.: Kung und R. Wu, Academic Press (1993), 128-43; Potrykus, Annu. Rev. Plant Physiol. Plant Molec. Biol. 42 (1991), 205-225; or mammalian cells. Suitable host cells are discussed further in Goeddel, Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990). Alternatively, the recombinant expression vector can be transcribed and translated in vitro, for example using T7 promoter regulatory sequences and T7 polymerase.

[0154] Expression of proteins in prokaryotes is most often carried out with vectors containing constitutive or inducible promoters directing the expression of either fusion or non-fusion proteins. Fusion vectors add a number of amino acids to a protein encoded therein, usually to the amino terminus of the recombinant protein but also to the C-terminus or fused within suitable regions in the proteins. Such fusion vectors typically serve three purposes: 1) to increase expression of recombinant protein; 2) to increase the solubility of the recombinant protein; and 3) to aid in the purification of the recombinant protein by acting as a ligand in affinity purification. Often, in fusion expression vectors, a proteolytic cleavage site is introduced at the junction of the fusion moiety and the recombinant protein to enable separation of the recombinant protein from the fusion moiety subsequent to purification of the fusion protein. Such enzymes, and their cognate recognition sequences, include Factor Xa, thrombin and enterokinase.

[0155] Typical fusion expression vectors include pGEX (Pharmacia Biotech Inc; Smith, D. B. and Johnson, K. S. (1988) Gene 67:31-40), pMAL (New England Biolabs, Beverly, Mass.) and pRIT5 (Pharmacia, Piscataway, N.J.) which fuse glutathione S-transferase (GST), maltose E binding protein, or protein A, respectively, to the target recombinant protein. In one embodiment, the coding sequence of the MP protein is cloned into a pGEX expression vector to create a vector encoding a fusion protein comprising, from the N-terminus to the C-terminus, GST-thrombin cleavage site-X protein. The fusion protein can be purified by affinity chromatography using glutathione-agarose resin. Recombinant MP protein unfused to GST can be recovered by cleavage of the fusion protein with thrombin.

[0156] Examples of suitable inducible non-fusion E. coli expression vectors include pTrc (Amann et al., (1988) Gene 69:301-315) and pET 11d (Studier et al., Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990) 60-89). Target gene expression from the pTrc vector relies on host RNA polymerase transcription from a hybrid trp-lac fusion promoter. Target gene expression from the pET 11d vector relies on transcription from a T7 gn10-lac fusion promoter mediated by a coexpressed viral RNA polymerase (T7 gn1). This viral polymerase is supplied by host strains BL21(DE3) or HMS174(DE3) from a resident λ prophage harboring a T7 gn1 gene under the transcriptional control of the lacUV 5 promoter.

[0157] One strategy to maximize recombinant protein expression is to express the protein in a host bacteria with an impaired capacity to proteolytically cleave the recombinant protein (Gottesman, S., Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990) 119-128). Another strategy is to alter the nucleic acid sequence of the nucleic acid to be inserted into an expression vector so that the individual codons for each amino acid are those preferentially utilized in the bacterium chosen for expression, such as C. glutamicum (Wada et al. (1992) Nucleic Acids Res. 20:2111-2118). Such alteration of nucleic acid sequences of the invention can be carried out by standard DNA synthesis techniques.

[0158] In another embodiment, the MP protein expression vector is a yeast expression vector. Examples of vectors for expression in yeast S. cerivisae include pYepSec1 (Baldari, et al., (1987) Embo J. 6:229-234), pMFa (Kujan and Herskowitz, (1982) Cell 30:933-943), pJRY88 (Schultz et al., (1987) Gene 54:113-123), and pYES2 (Invitrogen Corporation, San Diego, Calif.). Vectors and methods for the construction of vectors appropriate for use in other fungi, such as the filamentous fungi, include those detailed in: van den Hondel, C. A. M. J. J. & Punt, P. J. (1991) “Gene transfer systems and vector development for filamentous fungi, in: Applied Molecular Genetics of Fungi, J. F. Peberdy, et al., eds., p. 1-28, Cambridge University Press: Cambridge.

[0159] Alternatively, the MP proteins of the invention can be expressed in insect cells using baculovirus expression vectors. Baculovirus vectors available for expression of proteins in cultured insect cells (e.g., Sf 9 cells) include the pAc series (Smith et al. (1983) Mol. Cell Biol. 3:2156-2165) and the pVL series (Lucklow and Summers (1989) Virology 170:31-39).

[0160] In yet another embodiment, a nucleic acid of the invention is expressed in mammalian cells using a mammalian expression vector. Examples of mammalian expression vectors include pCDM8 (Seed, B. (1987) Nature 329:840) and pMT2PC (Kaufman et al. (1987) EMBOJ. 6:187-195). When used in mammalian cells, the expression vector's control functions are often provided by viral regulatory elements. For example, commonly used promoters are derived from polyoma, Adenovirus 2, cytomegalovirus and Simian Virus 40. For other suitable expression systems for both prokaryotic and eukaryotic cells see chapters 16 and 17 of Sambrook, J., Fritsh, E. F., and Maniatis, T. Molecular Cloning: A Laboratory Manual. 2nd, ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989.

[0161] In another embodiment, the recombinant mammalian expression vector is capable of directing expression of the nucleic acid preferentially in a particular cell type (e.g., tissue-specific regulatory elements are used to express the nucleic acid). Tissue-specific regulatory elements are known in the art. Non-limiting examples of suitable tissue-specific promoters include the albumin promoter (liver-specific; Pinkert et al. (1987) Genes Dev. 1:268-277), lymphoid-specific promoters (Calame and Eaton (1988) Adv. Immunol. 43:235-275), in particular promoters of T cell receptors (Winoto and Baltimore (1989) EMBO J 8:729-733) and immunoglobulins (Baneiji et al. (1983) Cell 33:729-740; Queen and Baltimore (1983) Cell 33:741-748), neuron-specific promoters (e.g., the neurofilament promoter; Byrne and Ruddle (1989) PNAS 86:5473-5477), pancreas-specific promoters (Edlund et al. (1985) Science 230:912-916), and mammary gland-specific promoters (e.g., milk whey promoter; U.S. Pat. No. 4,873,316 and European Application Publication No. 264,166). Developmentally-regulated promoters are also encompassed, for example the murine hox promoters (Kessel and Gruss (1990) Science 249:374-379) and the fetoprotein promoter (Campes and Tilghman (1989) Genes Dev. 3:537-546).

[0162] In another embodiment, the MP proteins of the invention may be expressed in unicellular plant cells (such as algae) see Falciatore et al., 1999, Marine Biotechnology.1 (3):239-251 and references therein and plant cells from higher plants (e.g., the spermatophytes, such as crop plants). Examples of plant expression vectors include those detailed in: Becker, D., Kemper, E., Schell, J. and Masterson, R. (1992) “New plant binary vectors with selectable markers located proximal to the left border”, Plant Mol. Biol. 20: 1195-1197; and Bevan, M. W. (1984) “Binary Agrobacterium vectors for plant transformation, Nucl. Acid. Res. 12: 8711-8721; Vectors for Gene Transfer in Higher Plants; in: Transgenic Plants, Vol. 1, Engineering and Utilization, eds.: Kung und R. Wu, Academic Press, 1993, S. 15-38.

[0163] A plant expression cassette preferably contains regulatory sequences capable to drive gene expression in plants cells and which are operably linked so that each sequence can fulfill its function such as termination of transcription such as polyadenylation signals. Preferred polyadenylation signals are those originating from Agrobacterium tumefaciens t-DNA such as the gene 3 known as octopine synthase of the Ti-plasmid pTiACH5 (Gielen et al., EMBO J. 3 (1984), 835 ff) or functional equivalents thereof but also all other terminators are suitable.

[0164] As plant gene expression is very often not limited on transcriptional levels a plant expression cassette preferably contains other operably linked sequences like translational enhancers such as the overdrive-sequence containing the 5′-untranslated leader sequence from tobacco mosaic virus enhancing the protein per RNA ratio (Gallie et al 1987, Nucl. Acids Research 15:8693-8711).

[0165] Plant gene expression has to be operably linked to an appropriate promoter conferring gene expression in a timely, cell or tissue specific manner. Preferred are promoters driving constitutitive expression (Benfey et al., EMBO J. 8 (1989) 2195-2202) like those derived from plant viruses like the 35S CAMV (Franck et al., Cell 21(1980) 285-294), the 19S CaMV (see also US5352605 and WO8402913) or plant promoters like those from Rubisco small subunit described in U.S. Pat. No. 4,962,028. WO 8705629, WO 9204449.

[0166] Other preferred sequences for use operable linkage in plant gene expression cassettes are targeting-sequences necessary to direct the gene-product in its appropriate cell compartment (for review see Kermode, Crit. Rev. Plant Sci. 15, 4 (1996), 285-423 and references cited therein) such as the vacuole, the nucleus, all types of plastids like amyloplasts, chloroplasts, chromoplasts, the extracellular space, mitochondria, the endoplasmic reticulum, oil bodies, peroxisomes and other compartments of plant cells.

[0167] Plant gene expression can also be facilitated via a chemically inducible promoter (for review see Gatz 1997, Annu. Rev. Plant Physiol. Plant Mol. Biol., 48:89-108). Chemically inducible promoters are especially suitable if gene expression is wanted to occur in a time specific manner. Examples for such promoters are a salicylic acid inducible promoter (WO 95/19443), a tetracycline inducible promoter (Gatz et al., (1992) Plant J. 2, 397-404) and an ethanol inducible promoter (WO 93/21334).

[0168] Also promoters responding to biotic or abiotic stress conditions are suitable promoters such as the pathogen inducible PRP1-gene promoter (Ward et al., Plant. Mol. Biol. 22 (1993), 361-366), the heat inducible hsp80-promoter from tomato (U.S. Pat. No. 5,187,267), cold inducible alpha-amylase promoter from potato (WO9612814) or the wound-inducible pinII-promoter (EP375091).

[0169] Especially those promoters are preferred which confer gene expression in storage tissues and organs such as cells of the endosperm and the developing embryo. Suitable promoters are the napin-gene promoter from rapeseed (U.S. Pat. No. 5,608,152), the USP-promoter from Vicia faba (Baeumlein et al., Mol Gen Genet, 1991, 225 (3):459-67), the oleosin-promoter from Arabidopsis (WO9845461), the phaseolin-promoter from Phaseolus vulgaris (U.S. Pat. No. 5,504,200), the Bce4-promoter from Brassica (WO9113980) or the legumin B4 promoter (LeB4; Baeumlein et al., 1992, Plant Journal, 2 (2):233-9) as well as promoters conferring seed specific expression in monocot plants like maize, barley, wheat, rye, rice etc. Suitable promoters to note are the lpt2 or lpt1-gene promoter from barley (WO9515389 and WO9523230) or those described in WO9916890 (promoters from the barley hordein-gene, the rice glutelin gene, the rice oryzin gene, the rice prolamin gene, the wheat gliadin gene, wheat glutelin gene, the maize zein gene, the oat glutelin gene, the Sorghum kasirin-gene, the rye secalin gene).

[0170] Also especially suited are promoters that confer plastid-specific gene expression as plastids are the compartment where part of the biosynthesis of amino acids, vitamins, cofactors, nutraceuticals, nucleotide or nucleosides take place. Suitable promoters such as the viral RNA-polymerase promoter are described in WO9516783 and WO9706250 and the clpP-promoter from Arabidopsis described in WO9946394.

[0171] The invention further provides a recombinant expression vector comprising a DNA molecule of the invention cloned into the expression vector in an antisense orientation. That is, the DNA molecule is operatively linked to a regulatory sequence in a manner which allows for expression (by transcription of the DNA molecule) of an RNA molecule which is antisense to MP mRNA. Regulatory sequences operatively linked to a nucleic acid cloned in the antisense orientation can be chosen which direct the continuous expression of the antisense RNA molecule in a variety of cell types, for instance viral promoters and/or enhancers, or regulatory sequences can be chosen which direct constitutive, tissue specific or cell type specific expression of antisense RNA. The antisense expression vector can be in the form of a recombinant plasmid, phagemid or attenuated virus in which antisense nucleic acids are produced under the control of a high efficiency regulatory region, the activity of which can be determined by the cell type into which the vector is introduced. For a discussion of the regulation of gene expression using antisense genes see Weintraub, H. et al., Antisense RNA as a molecular tool for genetic analysis, Reviews—Trends in Genetics, Vol. 1(1) 1986 and Mol et al., 1990, FEBS Letters 268:427-430.

[0172] Another aspect of the invention pertains to host cells into which a recombinant expression vector of the invention has been introduced. The terms “host cell” and “recombinant host cell” are used interchangeably herein. It is understood that such terms refer not only to the particular subject cell but to the progeny or potential progeny of such a cell. Because certain modifications may occur in succeeding generations due to either mutation or environmental influences, such progeny may not, in fact, be identical to the parent cell, but are still included within the scope of the term as used herein.

[0173] A host cell can be any prokaryotic or eukaryotic cell. For example, an MP protein can be expressed in bacterial cells such as E.coli, C. glutamicum, insect cells, fungal cells or mammalian cells (such as Chinese hamster ovary cells (CHO) or COS cells), algae, ciliates, plant cells or fungi. Other suitable host cells are known to those skilled in the art.

[0174] Vector DNA can be introduced into prokaryotic or eukaryotic cells via conventional transformation or transfection techniques. As used herein, the terms “transformation” and “transfection”, conjugation and transduction are intended to refer to a variety of art-recognized techniques for introducing foreign nucleic acid (e.g., DNA) into a host cell, including calcium phosphate or calcium chloride co-precipitation, DEAE-dextran-mediated transfection, lipofection, natural competence, chemical-mediated transfer, or electroporation. Suitable methods for transforming or transfecting host cells including plant cells can be found in Sambrook, et al. (Molecular Cloning: A Laboratory Manual. 2nd, ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989) and other laboratory manuals such as Methods in Molecular Biology, 1995, Vol. 44, Agrobacterium protocols, ed: Gartland and Davey, Humana Press, Totowa, N.J.

[0175] For stable transfection of mammalian cells, it is known that, depending upon the expression vector and transfection technique used, only a small fraction of cells may integrate the foreign DNA into their genome. In order to identify and select these integrants, a gene that encodes a selectable marker (e.g., resistance to antibiotics) is generally introduced into the host cells along with the gene of interest. Preferred selectable markers include those which confer resistance to drugs, such as G418, hygromycin and methotrexate or in plants that confer resistance towards a herbicide such as glyphosate or glufosinate. Nucleic acid encoding a selectable marker can be introduced into a host cell on the same vector as that encoding an MP protein or can be introduced on a separate vector. Cells stably transfected with the introduced nucleic acid can be identified by, for example, drug selection (e.g., cells that have incorporated the selectable marker gene will survive, while the other cells die).

[0176] To create a homologous recombinant microorganism, a vector is prepared which contains at least a portion of an MP gene into which a deletion, addition or substitution has been introduced to thereby alter, e.g., functionally disrupt, the MP gene. Preferably, this MP gene is a Physcomitrella patens MP gene, but it can be a homologue from a related plant or even from a mammalian, yeast, or insect source. In a preferred embodiment, the vector is designed such that, upon homologous recombination, the endogenous MP gene is functionally disrupted (i.e., no longer encodes a functional protein; also referred to as a knock-out vector). Alternatively, the vector can be designed such that, upon homologous recombination, the endogenous MP gene is mutated or otherwise altered but still encodes functional protein (e.g., the upstream regulatory region can be altered to thereby alter the expression of the endogenous MP protein). To create a point mutation via homologous recombination also DNA-RNA hybrids can be used known as chimeraplasty known from Cole-Strauss et al. 1999, Nucleic Acids Research 27(5):1323-1330 and Kmiec Gene therapy. 19999, American Scientist. 87(3):240-247.

[0177] Whereas in the homologous recombination vector, the altered portion of the MP gene is flanked at its 5′ and 3′ ends by additional nucleic acid of the MP gene to allow for homologous recombination to occur between the exogenous MP gene carried by the vector and an endogenous MP gene in a microorganism or plant. The additional flanking MP nucleic acid is of sufficient length for successful homologous recombination with the endogenous gene. Typically, several hundreds of basepairs up to kilobases of flanking DNA (both at the 5′ and 3′ ends) are included in the vector (see e.g., Thomas, K. R., and Capecchi, M. R. (1987) Cell 51: 503 for a description of homologous recombination vectors or Strepp et al., 1998, PNAS, 95 (8):4368-4373 for cDNA based recombination in Physcomitrella patens). The vector is introduced into a microorganism or plant cell (e.g., via polyethyleneglycol mediated DNA) and cells in which the introduced MP gene has homologously recombined with the endogenous MP gene are selected, using art-known techniques.

[0178] In another embodiment, recombinant microorganisms can be produced which contain selected systems which allow for regulated expression of the introduced gene. For example, inclusion of an MP gene on a vector placing it under control of the lac operon permits expression of the MP gene only in the presence of IPTG. Such regulatory systems are well known in the art.

[0179] A host cell of the invention, such as a prokaryotic or eukaryotic host cell in culture, can be used to produce (i.e., express) an MP protein. An alternate method can be applied in addition in plants by the direct transfer of DNA into developing flowers via electroporation or Agrobacterium medium gene transfer. Accordingly, the invention further provides methods for producing MP proteins using the host cells of the invention. In one embodiment, the method comprises culturing the host cell of invention (into which a recombinant expression vector encoding an MP protein has been introduced, or into which genome has been introduced a gene encoding a wild-type or altered MP protein) in a suitable medium until MP protein is produced. In another embodiment, the method further comprises isolating MP proteins from the medium or the host cell.

[0180] C. Isolated MP Proteins

[0181] Another aspect of the invention pertains to isolated MP proteins, and biologically active portions thereof. An “isolated” or “purified” protein or biologically active portion thereof is substantially free of cellular material when produced by recombinant DNA techniques, or chemical precursors or other chemicals when chemically synthesized. The language “substantially free of cellular material” includes preparations of MP protein in which the protein is separated from cellular components of the cells in which it is naturally or recombinantly produced. In one embodiment, the language “substantially free of cellular material” includes preparations of MP protein having less than about 30% (by dry weight) of non-MP protein (also referred to herein as a “contaminating protein”), more preferably less than about 20% of non-MP protein, still more preferably less than about 10% of non-MP protein, and most preferably less than about 5% non-MP protein. When the MP protein or biologically active portion thereof is recombinantly produced, it is also preferably substantially free of culture medium, i.e., culture medium represents less than about 20%, more preferably less than about 10%, and most preferably less than about 5% of the volume of the protein preparation. The language “substantially free of chemical precursors or other chemicals” includes preparations of MP protein in which the protein is separated from chemical precursors or other chemicals which are involved in the synthesis of the protein. In one embodiment, the language “substantially free of chemical precursors or other chemicals” includes preparations of MP protein having less than about 30% (by dry weight) of chemical precursors or non-MP protein chemicals, more preferably less than about 20% chemical precursors or non-MP protein chemicals, still more preferably less than about 10% chemical precursors or non-MP protein chemicals, and most preferably less than about 5% chemical precursors or non-MP protein chemicals. In preferred embodiments, isolated proteins or biologically active portions thereof lack contaminating proteins from the same organism from which the MP protein is derived. Typically, such proteins are produced by recombinant expression of, for example, a Physcomitrella patens MP protein in other plants than Physcomitrella patens or microorganisms such as C. glutamicum or ciliates, algae or fungi.

[0182] An isolated MP protein or a portion thereof of the invention can participate in the metabolism of amino acids, vitamins, cofactors, nutraceuticals, nucleotides or nucleosides in Physcomitrella patens, or has one or more of the activities set forth in Table 1. In preferred embodiments, the protein or portion thereof comprises an amino acid sequence which is sufficiently homologous to an amino acid sequence of Appendix B such that the protein or portion thereof maintains the ability to participate in the metabolism of fine chemicals like amino acids, vitamins, cofactors, nutraceuticals, nucleotides, or nucleosides in Physcomitrella patens. The portion of the protein is preferably a biologically active portion as described herein. In another preferred embodiment, an MP protein of the invention has an amino acid sequence shown in Appendix B. In yet another preferred embodiment, the MP protein has an amino acid sequence which is encoded by a nucleotide sequence which hybridizes, e.g., hybridizes under stringent conditions, to a nucleotide sequence of Appendix A. In still another preferred embodiment, the MP protein has an amino acid sequence which is encoded by a nucleotide sequence that is at least about 50-60%, preferably at least about 60-70%, more preferably at least about 70-80%, 80-90%, 90-95%, and even more preferably at least about 96%, 97%, 98%, 99% or more homologous to one of the amino acid sequences of Appendix B. The preferred MP proteinS of the present invention also preferably possess at least one of the MP protein activities described herein. For example, a preferred MP protein of the present invention includes an amino acid sequence encoded by a nucleotide sequence which hybridizes, e.g., hybridizes under stringent conditions, to a nucleotide sequence of Appendix A, and which can participate in the metabolism of amino acids, vitamins, cofactors, nutraceuticals, nucleotides or nucleosides in Physcomitrella patens, or which has one or more of the activities set forth in Table 1.

[0183] In other embodiments, the MP protein is substantially homologous to an amino acid sequence of Appendix B and retains the functional activity of the protein of one of the sequences of Appendix B yet differs in amino acid sequence due to natural variation or mutagenesis, as described in detail in subsection I above. Accordingly, in another embodiment, the MP protein is a protein which comprises an amino acid sequence which is at least about 50-60%, preferably at least about 60-70%, and more preferably at least about 70-80, 80-90, 90-95%, and most preferably at least about 96%, 97%, 98%, 99% or more homologous to an entire amino acid sequence of Appendix B and which has at least one of the MP protein activities described herein. In another embodiment, the invention pertains to a full Physcomitrella patens protein which is substantially homologous to an entire amino acid sequence of Appendix B.

[0184] Biologically active portions of an MP protein include peptides comprising amino acid sequences derived from the amino acid sequence of an MP protein, e.g., the an amino acid sequence shown in Appendix B or the amino acid sequence of a protein homologous to an MP protein, which include fewer amino acids than a full length MP protein or the full length protein which is homologous to an MP protein, and exhibit at least one activity of an MP protein. Typically, biologically active portions (peptides, e.g., peptides which are, for example, 5, 10, 15, 20, 30, 35, 36, 37, 38, 39, 40, 50, 100 or more amino acids in length) comprise a domain or motif with at least one activity of an MP protein. Moreover, other biologically active portions, in which other regions of the protein are deleted, can be prepared by recombinant techniques and evaluated for one or more of the activities described herein. Preferably, the biologically active portions of an MP protein include one or more selected domains/motifs or portions thereof having biological activity.

[0185] MP proteins are preferably produced by recombinant DNA techniques. For example, a nucleic acid molecule encoding the protein is cloned into an expression vector (as described above), the expression vector is introduced into a host cell (as described above) and the MP protein is expressed in the host cell. The MP protein can then be isolated from the cells by an appropriate purification scheme using standard protein purification techniques. Alternative to recombinant expression, an MP protein, polypeptide, or peptide can be synthesized chemically using standard peptide synthesis techniques. Moreover, native MP protein can be isolated from cells (e.g., endothelial cells), for example using an anti-MP protein antibody, which can be produced by standard techniques utilizing an MP protein or fragment thereof of this invention.

[0186] The invention also provides MP protein chimeric or fusion proteins. As used herein, an MP “chimeric protein” or “fusion protein” comprises an MP polypeptide operatively linked to a non-MP polypeptide. An “MP polypeptide” refers to a polypeptide having an amino acid sequence corresponding to an MP protein, whereas a “non-MP polypeptide” refers to a polypeptide having an amino acid sequence corresponding to a protein which is not substantially homologous to the MP protein, e.g., a protein which is different from the MP protein and which is derived from the same or a different organism. Within the fusion protein, the term “operatively linked” is intended to indicate that the MP polypeptide and the non-MP polypeptide are fused to each other so that both sequences fulfill the proposed function addicted to the sequence used. The non-MP polypeptide can be fused to the N-terminus or C-terminus of the MP polypeptide. For example, in one embodiment the fusion protein is a GST-MP fusion protein in which the MP protein sequences are fused to the C-terminus of the GST sequences. Such fusion proteins can facilitate the purification of recombinant MP proteins. In another embodiment, the fusion protein is an MP protein containing a heterologous signal sequence at its N-terminus. In certain host cells (e.g., mammalian host cells), expression and/or secretion of an MP protein can be increased through use of a heterologous signal sequence.

[0187] Preferably, an MP chimeric or fusion protein of the invention is produced by standard recombinant DNA techniques. For example, DNA fragments coding for the different polypeptide sequences are ligated together in-frame in accordance with conventional techniques, for example by employing blunt-ended or stagger-ended termini for ligation, restriction enzyme digestion to provide for appropriate termini, filling-in of cohesive ends as appropriate, alkaline phosphatase treatment to avoid undesirable joining, and enzymatic ligation. In another embodiment, the fusion gene can be synthesized by conventional techniques including automated DNA synthesizers. Alternatively, PCR amplification of gene fragments can be carried out using anchor primers which give rise to complementary overhangs between two consecutive gene fragments which can subsequently be annealed and reamplified to generate a chimeric gene sequence (see, for example, Current Protocols in Molecular Biology, eds. Ausubel et al. John Wiley & Sons: 1992). Moreover, many expression vectors are commercially available that already encode a fusion moiety (e.g., a GST polypeptide). An MP protein-encoding nucleic acid can be cloned into such an expression vector such that the fusion moiety is linked in-frame to the MP protein.

[0188] Homologues of the MP protein can be generated by mutagenesis, e.g., discrete point mutation or truncation of the MP protein. As used herein, the term “homologue” refers to a variant form of the MP protein which acts as an agonist or antagonist of the activity of the MP protein. An agonist of the MP protein can retain substantially the same, or a subset, of the biological activities of the MP protein. An antagonist of the MP protein can inhibit one or more of the activities of the naturally occurring form of the MP protein, by, for example, competitively binding to a downstream or upstream member of the cell membrane component metabolic cascade which includes the MP protein, or by binding to an MP protein which mediates transport of compounds across such membranes, thereby preventing translocation from taking place.

[0189] In an alternative embodiment, homologues of the MP protein can be identified by screening combinatorial libraries of mutants, e.g., truncation mutants, of the MP protein for MP protein agonist or antagonist activity. In one embodiment, a variegated library of MP protein variants is generated by combinatorial mutagenesis at the nucleic acid level and is encoded by a variegated gene library. A variegated library of MP protein variants can be produced by, for example, enzymatically ligating a mixture of synthetic oligonucleotides into gene sequences such that a degenerate set of potential MP protein sequences is expressible as individual polypeptides, or alternatively, as a set of larger fusion proteins (e.g., for phage display) containing the set of MP protein sequences therein. There are a variety of methods which can be used to produce libraries of potential MP protein homologues from a degenerate oligonucleotide sequence. Chemical synthesis of a degenerate gene sequence can be performed in an automatic DNA synthesizer, and the synthetic gene then ligated into an appropriate expression vector. Use of a degenerate set of genes allows for the provision, in one mixture, of all of the sequences encoding the desired set of potential MP protein sequences. Methods for synthesizing degenerate oligonucleotides are known in the art (see, e.g., Narang, S. A. (1983) Tetrahedron 39:3; Itakura et al. (1984) Annu. Rev. Biochem. 53:323; Itakura et al. (1984) Science 198:1056; Ike et al. (1983) Nucleic Acid Res. 11:477.

[0190] In addition, libraries of fragments of the MP protein coding can be used to generate a variegated population of MP protein fragments for screening and subsequent selection of homologues of an MP protein. In one embodiment, a library of coding sequence fragments can be generated by treating a double stranded PCR fragment of an MP protein coding sequence with a nuclease under conditions wherein nicking occurs only about once per molecule, denaturing the double stranded DNA, renaturing the DNA to form double stranded DNA which can include sense/antisense pairs from different nicked products, removing single stranded portions from reformed duplexes by treatment with S1 nuclease, and ligating the resulting fragment library into an expression vector. By this method, an expression library can be derived which encodes N-terminal, C-terminal and internal fragments of various sizes of the MP protein.

[0191] Several techniques are known in the art for screening gene products of combinatorial libraries made by point mutations or truncation, and for screening cDNA libraries for gene products having a selected property. Such techniques are adaptable for rapid screening of the gene libraries generated by the combinatorial mutagenesis of MP protein homologues. The most widely used techniques, which are amenable to high through-put analysis, for screening large gene libraries typically include cloning the gene library into replicable expression vectors, transforming appropriate cells with the resulting library of vectors, and expressing the combinatorial genes under conditions in which detection of a desired activity facilitates isolation of the vector encoding the gene whose product was detected. Recursive ensemble mutagenesis (REM), a new technique which enhances the frequency of functional mutants in the libraries, can be used in combination with the screening assays to identify MP protein homologues (Arkin and Yourvan (1992) PNAS 89:7811-7815; Delgrave et al. (1993) Protein Engineering 6(3):327-331).

[0192] In another embodiment, cell based assays can be exploited to analyze a variegated MP protein library, using methods well known in the art.

[0193] D. Uses and Methods of the Invention

[0194] The nucleic acid molecules, proteins, protein homologues, fusion proteins, primers, vectors, and host cells described herein can be used in one or more of the following methods: identification of Physcomitrella patens and related organisms; mapping of genomes of organisms related to Physcomitrella patens; identification and localization of Physcomitrella patens sequences of interest; evolutionary studies; determination of MP protein regions required for function; modulation of an MP protein activity; modulation of the cellular production of one or more fine chemicals such as amino acids, vitamins, cofactors, nutraceuticals, nucleotides or nucleosides. The MP nucleic acid molecules of the invention have a variety of uses. First, they may be used to identify an organism as being Physcomitrella patens or a close relative thereof. Also, they may be used to identify the presence of Physcomitrella patens or a relative thereof in a mixed population of microorganisms. The invention provides the nucleic acid sequences of a number of Physcomitrella patens genes; by probing the extracted genomic DNA of a culture of a unique or mixed population of microorganisms under stringent conditions with a probe spanning a region of a Physcomitrella patens gene which is unique to this organism, one can ascertain whether this organism is present.

[0195] Further, the nucleic acid and protein molecules of the invention may serve as markers for specific regions of the genome. This has utility not only in the mapping of the genome, but also for functional studies of Physcomitrella patens proteins. For example, to identify the region of the genome to which a particular Physcomitrella patens DNA-binding protein binds, the Physcomitrella patens genome could be digested, and the fragments incubated with the DNA-binding protein. Those which bind the protein may be additionally probed with the nucleic acid molecules of the invention, preferably with readily detectable labels; binding of such a nucleic acid molecule to the genome fragment enables the localization of the fragment to the genome map of Physcomitrella patens, and, when performed multiple times with different enzymes, facilitates a rapid determination of the nucleic acid sequence to which the protein binds. Further, the nucleic acid molecules of the invention may be sufficiently homologous to the sequences of related species such that these nucleic acid molecules may serve as markers for the construction of a genomic map in related mosses, such as Physcomitrella patens.

[0196] The MP nucleic acid molecules of the invention are also useful for evolutionary and protein structural studies. The metabolic and transport processes in which the molecules of the invention participate are utilized by a wide variety of prokaryotic and eukaryotic cells; by comparing the sequences of the nucleic acid molecules of the present invention to those encoding similar enzymes from other organisms, the evolutionary relatedness of the organisms can be assessed. Similarly, such a comparison permits an assessment of which regions of the sequence are conserved and which are not, which may aid in determining those regions of the protein which are essential for the functioning of the enzyme. This type of determination is of value for protein engineering studies and may give an indication of what the protein can tolerate in terms of mutagenesis without losing function.

[0197] Manipulation of the MP nucleic acid molecules of the invention may result in the production of MP proteins having functional differences from the wild-type MP proteins. These proteins may be improved in efficiency or activity, may be present in greater numbers in the cell than is usual, or may be decreased in efficiency or activity.

[0198] There are a number of mechanisms by which the alteration of an MP protein of the invention may directly affect the yield, production, and/or efficiency of production of a fine chemical incorporating such an altered protein. Recovery of fine chemical compounds from large-scale cultures of C. glutamicum, ciliates, algae or fungi is significantly improved if the cell secretes the desired compounds, since such compounds may be readily purified from the culture medium (as opposed to extracted from the mass of cultured cells). In the case of plants expressing MP proteins increased transport can lead to improved partitioning within the plant tissue and organs. By either increasing the number or the activity of transporter molecules which export fine chemicals from the cell, it may be possible to increase the amount of the produced fine chemical which is present in the extracellular medium, thus permitting greater ease of harvesting and purification or in case of plants mor efficient partitioning. Conversely, in order to efficiently overproduce one or more fine chemicals, increased amounts of the cofactors, precursor molecules, and intermediate compounds for the appropriate biosynthetic pathways are required. Therefore, by increasing the number and/or activity of transporter proteins involved in the import of nutrients, such as carbon sources (i.e., sugars), nitrogen sources (i.e., amino acids, ammonium salts), phosphate, and sulfur, it may be possible to improve the production of a fine chemical, due to the removal of any nutrient supply limitations on the biosynthetic process.

[0199] The engineering of one or more MP genes of the invention may also result in MP proteins having altered activities which indirectly impact the production of one or more desired fine chemicals from algae, plants, ciliates or fungi or other microorganisms like C. glutamicum. For example, the normal biochemical processes of metabolism result in the production of a variety of waste products (e.g., hydrogen peroxide and other reactive oxygen species) which may actively interfere with these same metabolic processes (for example, peroxynitrite is known to nitrate tyrosine side chains, thereby inactivating some enzymes having tyrosine in the active site (Groves, J. T. (1999) Curr. Opin. Chem. Biol 3(2): 226-235). While these waste products are typically excreted, cells utilized for large-scale fermentative production are optimized for the overproduction of one or more fine chemicals, and thus may produce more waste products than is typical for a wild-type cell. By optimizing the activity of one or more MP proteins of the invention which are involved in the export of waste molecules, it may be possible to improve the viability of the cell and to maintain efficient metabolic activity. Also, the presence of high intracellular levels of the desired fine chemical may actually be toxic to the cell, so by increasing the ability of the cell to secrete these compounds, one may improve the viability of the cell.

[0200] Further, the MP proteins of the invention may be manipulated such that the relative amounts of various lipophilic fine chemicals like for example vitamin E or carotenoids are altered. This may have a profound effect on the lipid composition of the membrane of the cell. Since each type of lipid has different physical properties, an alteration in the lipid composition of a membrane may significantly alter membrane fluidity. Changes in membrane fluidity can impact the transport of molecules across the membrane, which, as previously explicated, may modify the export of waste products or the produced fine chemical or the import of necessary nutrients. Such membrane fluidity changes may also profoundly affect the integrity of the cell; cells with relatively weaker membranes are more vulnerable abiotic and biotic stress conditions which may damage or kill the cell. By manipulating MP proteins involved in the production of lipophilic fine chemicals for membrane construction such that the resulting membrane has a membrane composition more amenable to the environmental conditions extant in the cultures utilized to produce fine chemicals, a greater proportion of the cells should survive and multiply. Greater numbers of producing cells should translate into greater yields, production, or efficiency of production of the fine chemical from the culture.

[0201] The aforementioned mutagenesis strategies for MP proteins to result in increased yields of a fine chemical are not meant to be limiting; variations on these strategies will be readily apparent to one skilled in the art. Using such strategies, and incorporating the mechanisms disclosed herein, the nucleic acid and protein molecules of the invention may be utilized to generate algae, ciliates, plants, fungi or other microorganisms like C. glutamicum expressing mutated MP nucleic acid and protein molecules such that the yield, production, and/or efficiency of production of a desired compound is improved. This desired compound may be any natural product of algae, ciliates, plants, fungi or C. glutamicum, which includes the final products of biosynthesis pathways and intermediates of naturally-occurring metabolic pathways, as well as molecules which do not naturally occur in the metabolism of said cells, but which are produced by a said cells of the invention.

[0202] This invention is further illustrated by the following examples which should not be construed as limiting. The contents of all references, patent applications, patents, and published patent applications cited throughout this application are hereby incorporated by reference.

EXAMPLIFICATION Example 1

[0203] General Processes

[0204] a) General Cloning Processes

[0205] Cloning processes such as, for example, restriction cleavages, agarose gel electrophoresis, purification of DNA fragments, transfer of nucleic acids to nitrocellulose and nylon membranes, linkage of DNA fragments, transformation of Escherichia coli and yeast cells, growth of bacteria and sequence analysis of recombinant DNA were carried out as described in Sambrook et al. (1989) (Cold Spring Harbor Laboratory Press: ISBN 0-87969-309-6) or Kaiser, Michaelis and Mitchell (1994) “Methods in Yeasr Genetics” (Cold Spring Harbor Laboratory Press: ISBN 0-87969-451-3). Transformation and cultivation 21of algae such as Chlorella or Phaeodactylum are transformed as described by El-Sheekh (1999), Biologia Plantarum 42: 209-216; Apt et al. (1996), Molecular and General Genetics 252 (5): 872-9.

[0206] b) Chemicals

[0207] The chemicals used were obtained, if not mentioned otherwise in the text, in p.a. quality from the companies Fluka (Neu-Ulm), Merck (Darmstadt), Roth (Karlsruhe), Serva (Heidelberg) and Sigma (Deisenhofen). Solutions were prepared using purified, pyrogen-free water, designated as H₂O in the following text, from a Milli-Q water system water purification plant (Millipore, Eschborn). Restriction endonucleases, DNA-modifying enzymes and molecular biology kits were obtained from the companies AGS (Heidelberg), Amersham (Braunschweig), Biometra (Göttingen), Boehringer (Mannheim), Genomed (Bad Oeynnhausen), New England Biolabs (Schwalbach/Taunus), Novagen (Madison, Wis., USA), Perkin-Elmer (Weiterstadt), Pharmacia (Freiburg), Qiagen (Hilden) and Stratagene (Amsterdam, Netherlands). They were used, if not mentioned otherwise, according to the manufacturer's instructions.

[0208] c) Plant Material

[0209] For this study, plants of the species Physcoritrella patens (Hedw.) B.S.G. from the collection of the genetic studies section of the University of Hamburg were used. They originate from the strain 16/14 collected by H. L. K. Whitehouse in Gransden Wood, Huntingdonshire (England), which was subcultured from a spore by Engel (1968, Am J Bot 55, 438-446). Proliferation of the plants was carried out by means of spores and by means of regeneration of the gametophytes. The protonema developed from the haploid spore as a chloroplast-rich chloronema and chloroplast-low caulonema, on which buds formed after approximately 12 days. These grew to give gametophores bearing antheridia and archegonia. After fertilization, the diploid sporophyte with a short seta and the spore capsule resulted, in which the meiospores mature.

[0210] d) Plant Growth

[0211] Culturing was carried out in a climatic chamber at an air temperature of 25□ C. and light intensity of 55 micromols-1m-2 (white light; Philips TL 65W/25 fluorescent tube) and a light/dark change of 16/8 hours. The moss was either modified in liquid culture using Knop medium according to Reski and Abel (1985, Planta 165, 354-358) or cultured on Knop solid medium using 1% oxoid agar (Unipath, Basingstoke, England). The protonemas used for RNA and DNA isolation were cultured in aerated liquid cultures. The protonemas were comminuted every 9 days and transferred to fresh culture medium.

Example 2

[0212] Total DNA Isolation from Plants

[0213] The details for the isolation of total DNA relate to the working up of one gram fresh weight of plant material.

[0214] CTAB buffer: 2% (w/v) N-cethyl-N,N,N-trimethylammonium bromide (CTAB); 100 mM Tris HCl pH 8.0; 1.4 M NaCl; 20 mM EDTA.

[0215] N-Laurylsarcosine buffer: 10% (w/v) N-laurylsarcosine; 100 mM Tris HCl pH 8.0; 20 mM EDTA.

[0216] The plant material was triturated under liquid nitrogen in a mortar to give a fine powder and transferred to 2 ml Eppendorf vessels. The frozen plant material was then covered with a layer of 1 ml of decomposition buffer (1 ml CTAB buffer, 100 ml of N-laurylsarcosine buffer, 20 ml of b-mercaptoethanol and 10 ml of proteinase K solution, 10 mg/ml) and incubated at 60□ C. for one hour with continuous shaking. The homogenate obtained was distributed into two Eppendorf vessels (2 ml) and extracted twice by shaking with the same volume of chloroform/isoamyl alcohol (24:1). For phase separation, centrifugation was carried out at 8000×g and RT for 15 min in each case. The DNA was then precipitated at −70□ C. for 30 min using ice-cold isopropanol. The precipitated DNA was sedimented at 4□ C. and 10,000 g for 30 min and resuspended in 180 ml of TE buffer (Sambrook et al., 1989, Cold Spring Harbor Laboratory Press: ISBN 0-87969-309-6). For further purification, the DNA was treated with NaCl (1.2 M final concentration) and precipitated again at −70□ C. for 30 min using twice the volume of absolute ethanol. After a washing step with 70% ethanol, the DNA was dried and subsequently taken up in 50 ml of H₂O+RNAse (50 mg/ml final concentration). The DNA was dissolved overnight at 40□ C. and the RNAse digestion was subsequently carried out at 37□ C. for 1 h. Storage of the DNA took place at 4□ C.

Example 3

[0217] Isolation of Total RNA and Poly-(A)+ RNA from Plants

[0218] For the investigation of transcripts, both total RNA and poly-(A)⁺ RNA were isolated. The total RNA was obtained from wild-type 9d old protonemata following the GTC-method (Reski et al. 1994, Mol. Gen. Genet., 244:352-359).

[0219] Isolation of PolyA+ RNA was isolated using Dyna Beads® (Dynal, Oslo) Following the instructions of the manufacturers protocol. After determination of the concentration of the RNA or of the poly-(A)+ RNA, the RNA was precipitated by addition of {fraction (1/10)} volumes of 3 M sodium acetate pH 4.6 and 2 volumes of ehanol and stored at −70□ C.

Example 4

[0220] cDNA Library Construction

[0221] For cDNA library construction first strand synthesis was achieved using Murine Leukemia Virus reverse transcriptase (Roche, Mannheim, Germany) and olido-d(T)-primers, second strand synthesis by incubation with DNA polymerase I, Klenow enzyme and RNAseH digestion at 12° C. (2 h), 16° C. (1 h) and 22° C. (1 h). The reaction was stopped by incubation at 65° C. (10 min) and subsequently transferred to ice. Double stranded DNA molecules were blunted by T4-DNA-polymerase (Roche, Mannheim) at 37° C. (30 min). Nucleotides were removed by phenol/chloroform extraction and Sephadex-G50 spin columns. EcoRI adapters (Pharmacia, Freiburg, Germany) were ligated to the cDNA ends by T4-DNA-ligase (Roche, 12° C., overnight) and phosphorylated by incubation with polynucleotide kinase (Roche, 37° C., 30 min). This mixture was subjected to separation on a low melting agarose gel. DNA molecules larger than 300 basepairs were eluted from the gel, phenol extracted, concentrated on Elutip-D-columns (Schleicher and Schuell, Dassel, Germany) and were ligated to vector arms and packed into lambda ZAPII—phages or lambda ZAP-Express phages using the Gigapack Gold Kit (Stratagene, Amsterdam, Netherlands) using material and following the instructions of the manufacturer.

Example 5

[0222] Identification of Genes of Interest

[0223] Gene sequences can be used to identify homologous or heterologous genes from cDNA or genomic libraries.

[0224] Homologous genes (e. g. full length cDNA clones) can be isolated via nucleic acid hybridization using for example cDNA libraries: Depended on the abundance of the gene of interest 100,000 up to 1,000,000 recombinant bacteriophages are plated and transferred to a nylon membrane. After denaturation with alkali, DNA is immobilized on the membrane by e.g. UV cross linking. Hybridization is carried out at high stringency conditions. In aqueous solution hybridization and washing is performed at an ionic strength of 1 M NaCl and a temperature of 68□ C. Hybridization probes are generated by e.g. radioactive (³²P) nick transcription labeling (Amersham Ready Prime). Signals are detected by exposure to x-ray films.

[0225] Partially homologous or heterologous genes that are related but not identical can be identified analog to the above described procedure using low stringency hybridization and washing conditions. For aqueous hybridization the ionic strength is normally kept at 1 M NaCl while the temperature is progressively lowered from 68 to 42□ C.

[0226] Isolation of gene sequences with homologies only in a distinct domain of (for example 20 amino acids) can be carried out by using synthetic radio labeled oligonucleotide probes. Radio labeled oligonucleotides are prepared by phosphorylalation of the 5′-prime end of two complementary oligonucleotides with T4 polynucleotede kinase. The complementary oligonucleotides are annealed and ligated to form concatemers. The double stranded concatemers are than radiolabled by for example nick transcription. Hybridization is normally performed at low stringency conditions using high oligonucleotide concentrations.

[0227] Oligonucleotide hybridization solution:

[0228] 6×SSC

[0229] 0.01 M sodium phosphate

[0230] 1 mM EDTA (pH 8)

[0231] 0.5% SDS

[0232] 100 μg/ml denaturated salmon sperm DNA

[0233] 0.1% nonfat dried milk

[0234] During hybridization temperature is lowered stepwise to 5-10□ C. below the estimated oligonucleotid Tm.

[0235] Further details are described by Sambrook, J. et al. (1989), “Molecular Cloning: A Laboratory Manual”, Cold Spring Harbor Laboratory Press or Ausubel, F. M. et al. (1994) “Current Protocols in Molecular Biology”, John Wiley & Sons.

Example 6

[0236] Identification of Genes of Interest by Screening Expression Libraries with Antibodies

[0237] C-DNA sequences can be used to produce recombinant protein for example in E. coli (e.g. Qiagen QIAexpress pQE system). Recombinant proteins are than normally affinity purified via Ni-NTA affinity chromatoraphy (Qiagen). Recombinant proteins are than used to produce specific antibodies for example by using standard techniques for rabbit immunization. Antibodies are affinity purified using a Ni-NTA column saturated with the recombinant antigen as described by Gu et al., (1994) BioTechniques 17: 257-262. The antibody can than be used to screen expression cDNA libraries to identify homologous or heterologous genes via an immunological screening (Sambrook, J. et al. (1989), “Molecular Cloning: A Laboratory Manual”, Cold Spring Harbor Laboratory Press or Ausubel, F. M. et al. (1994) “Current Protocols in Molecular Biology”, John Wiley & Sons).

Example 7

[0238] Northern-hybridization

[0239] For RNA hybridization, 20 mg of total RNA or 1 mg of poly-(A)+ RNA were separated by gel electrophoresis in 1.25% strength agarose gels using formaldehyde as described in Amasino (1986, Anal. Biochem. 152, 304), transferred by capillary attraction using 10×SSC to positively charged nylon membranes (Hybond N+, Amersham, Braunschweig), immobilized by UV light and prehybridized for 3 hours at 68° C. using hybridization buffer (10% dextran sulfate w/v, 1 M NaCl, 1% SDS, 100 mg of herring sperm DNA). The labeling of the DNA probe with the “Highprime DNA labeling kit” (Roche, Mannheim, Germany) was carried out during the prehybridization using alpha-³²P dCTP (Amersham, Braunschweig, Germany). Hybridization was carried out after addition of the labeled DNA probe in the same buffer at 68° C. overnight. The washing steps were carried out twice for 15 min using 2×SSC and twice for 30 min using 1×SSC, 1% SDS at 68° C. The exposure of the sealed-in filters was carried out at −70° C. for a period of 1-14d.

Example 8

[0240] DNA Sequencing and Computational Functional Analysis

[0241] CDNA libraries libraries as described in Example 4 were used for DNA sequencing according to standard methods, in particular by the chain termination method using the ABI PRISM Big Dye Terminator Cycle Sequencing Ready Reaction Kit (Perkin-Elmer, Weiterstadt, Germany). Random Sequencing was carried out subsequent to preparative plasmid recovery from cDNA libraries via in vivo mass excision and retransformation of DH10B on agar plates (material and protocol details from Stratagene, Amsterdam, Netherlands. Plasmid DNA was prepared from overnight grown E. coli cultures grown in Luria-Broth medium containing ampicillin (see Sambrook et al. (1989) (Cold Spring Harbor Laboratory Press: ISBN 0-87969-309-6)) on a Qiagene DNA preparation robot (Qiagen, Hilden) according to the manufacturers protocols. Sequencing primers with the following nucleotide sequences were used: 5′-CAGGAAACAGCTATGACC-3′ 5′-CTAAAGGGAACAAAAGCTG-3′ 5′-TGTAAAACGACGGCCAGT-3′

Example 9

[0242] Plasmids for Plant Transformation

[0243] For plant transformation binary vectors such as pBinAR can be used (Höfgen and Willmitzer, Plant Science 66(1990), 221-230). Construction of the binary vectors can be performed by ligation of the cDNA in sense or antisense orientation into the T-DNA. 5′-prime to the cDNA a plant promotor activates transcription of the cDNA. A polyadenylation sequence is located 3′-prime to the cDNA.

[0244] Tissue specific expression can be archived by using a tissue specific promotor. For example seed specific expression can be archived by cloning the napin or USP promotor 5-prime to the cDNA. Also any other seed specific promotor element can be used. For constitutive expression within the whole plant the CaMV 35S promotor can be used.

[0245] The expressed protein can be targeted to a cellular compartment using a signal peptide, for example for plasids, mitochondria or endoplasmatic reticulum (Kermode, Crit. Rev. Plant Sci. 15, 4 (1996), 285-423). The signal peptide is cloned 5′-prime in frame to the cDNA to archive subcellular localization of the fusionprotein.

[0246] Nucleic acid molecules from Physcomitrella are used for a direct gene knock-out by homologous recombination. Therefore Physcometrella sequences are usefull for functional genomic approaches. The technique is described by Strepp et al., Proc. Natl. Acad. Sci. USA, 1998, 95: 4369-4373; Girke et al. (1998), Plant Journal 15: 39-48; Hoffman et al. (1999) Molecular and General Genetics 261: 92-99.

Example 10

[0247] Transformation of Agrobacterium

[0248] Agrobacterium mediated plant transformation can be performed using for example the GV3101(pMP90) (Koncz and Schell, Mol. Gen. Genet. 204 (1986), 383-396) or LBA4404 (Clontech) Agrobacterium tumefaciens strain. Transformation can be performed by standard transformation techniques (Deblaere et al., Nucl. Acids. Tes. 13 (1984), 4777-4788).

Example 11

[0249] Plant Transformation

[0250] Agrobacterium mediated plant transformation has been performed using standard transformation and regeneration techniques (Gelvin, Stanton B.; Schilperoort, Robert A, “Plant Molecular Biology Manual”, 2nd Ed.-Dordrecht: Kluwer Academic Publ., 1995. -in Sect., Ringbuc Zentrale Signatur: BT11-P ISBN 0-7923-2731-4; Glick, Bernard R.; Thompson, John E., “Methods in Plant Molecular Biology and Biotechnology”, Boca Raton: CRC Press, 1993.-360 S.,ISBN 0-8493-5164-2).

[0251] For example rapeseed can be transformed via cotyledon or hypocotyl transformation (Moloney et al., Plant cell Report 8 (1989), 238-242; De Block et al., Plant Physiol. 91 (1989, 694-701). Use of antibiotica for agrobacterium and plant selection depends on the binary vector and the agrobacterium strain used for transformation. Rapeseed selection is normally performed using kanamycin as selectable plant marker.

[0252] Agrobacterium mediated gene transfer to flax can be performed using for example a technique described by Mlynarova et al. (1994), Plant Cell Report 13: 282-285.

[0253] Transformation of soybean can be performed using for example a technique described in EP 0424 047, U.S. Pat. No. 322,783 (Pioneer Hi-Bred International) or in EP 0397 687, U.S. Pat. No. 5,376,543, U.S. Pat. No. 5,169,770 (University Toledo).

[0254] Plant transformation using particle bombardment, Polyethylene Glycol mediated DNA uptake or via the Silicon Carbide Fiber technique is for example described by Freeling and Walbot “The maize handbook” (1993) ISBN 3-540-97826-7, Springer Verlag New York).

Example 12

[0255] In Vivo Mutagenesis

[0256] In vivo mutagenesis of microorganisms can be performed by passage of plasmid (or other vector) DNA through E. coli or other microorganisms (e.g. Bacillus spp. or yeasts such as Saccharomyces cerevisiae) which are impaired in their capabilities to maintain the integrity of their genetic information. Typical mutator strains have mutations in the genes for the DNA repair system (e.g., mutHLS, mutD, mutT, etc.; for reference, see Rupp, W. D. (1996) DNA repair mechanisms, in: Escherichia coli and Salmonella, p. 2277-2294, ASM: Washington.) Such strains are well known to those skilled in the art. The use of such strains is illustrated, for example, in Greener, A. and Callahan, M. (1994) Strategies 7: 32-34. Transfer of mutated DNA molecules into plants is preferably done after selection and testing in microorganisms. Transgenic plants are generated according to various examples within the exemplification of this document.

Example 13

[0257] DNA Transfer Between Escherichia Coli and Corynebacterium Glutamicum

[0258] Several Corynebacterium and Brevibacterium species contain endogenous plasmids (as e.g., pHM1519 or pBL1) which replicate autonomously (for review see, e.g., Martin, J. F. et al. (1987) Biotechnology, 5:137-146). Shuttle vectors for Escherichia coli and Corynebacterium glutamicum can be readily constructed by using standard vectors for E. coli (Sambrook, J. et al. (1989), “Molecular Cloning: A Laboratory Manual”, Cold Spring Harbor Laboratory Press or Ausubel, F. M. et al. (1994) “Current Protocols in Molecular Biology”, John Wiley & Sons) to which a origin or replication for and a suitable marker from Corynebacterium glutamicum is added. Such origins of replication are preferably taken from endogenous plasmids isolated from Corynebacterium and Brevibacterium species. Of particular use as transformation markers for these species are genes for kanamycin resistance (such as those derived from the Tn5 or Tn903 transposons) or chloramphenicol (Winnacker, E. L. (1987) “From Genes to Clones—Introduction to Gene Technology, VCH, Weinheim). There are numerous examples in the literature of the construction of a wide variety of shuttle vectors which replicate in both E. coli and C. glutamicum, and which can be used for several purposes, including gene over-expression (for reference, see e.g., Yoshihama, M. et al. (1985) J. Bacteriol. 162:591-597, Martin J. F. et al. (1987) Biotechnology, 5:137-146 and Eikmanns, B. J. et al. (1991) Gene, 102:93-98). Using standard methods, it is possible to clone a gene of interest into one of the shuttle vectors described above and to introduce such a hybrid vectors into strains of Corynebacterium glutamicum. Transformation of C. glutamicum can be achieved by protoplast transformation (Kastsumata, R. et al. (1984) J. Bacteriol. 159306-311), electroporation (Liebl, E. et al. (1989) FEMS Microbiol. Letters, 53:399-303) and in cases where special vectors are used, also by conjugation (as described e.g. in Schäfer, A et al. (1990) J. Bacteriol. 172:1663-1666). It is also possible to transfer the shuttle vectors for C. glutamicum to E. coli by preparing plasmid DNA from C. glutamicum (using standard methods well-known in the art) and transforming it into E. coli. This transformation step can be performed using standard methods, but it is advantageous to use an Mcr-deficient E. coli strain, such as NM522 (Gough & Murray (1983) J. Mol. Biol. 166:1-19).

Example 14

[0259] Assessment of the Expression of a Recombinant Gene Product in a Transformed Organism

[0260] The activity of a recombinant gene product in the transformed host organism has been measured on the transcriptional or/and on the translational level.

[0261] A useful method to ascertain the level of transcription of the gene (an indicator of the amount of mRNA available for translation to the gene product) is to perform a Northern blot (for reference see, for example, Ausubel et al. (1988) Current Protocols in Molecular Biology, Wiley: New York), in which a primer designed to bind to the gene of interest is labeled with a detectable tag (usually radioactive or chemiluminescent), such that when the total RNA of a culture of the organism is extracted, run on gel, transferred to a stable matrix and incubated with this probe, the binding and quantity of binding of the probe indicates the presence and also the quantity of mRNA for this gene. This information is evidence of the degree of transcription of the transformed gene. Total cellular RNA can be prepared from cells, tissues or organs by several methods, all well-known in the art, such as that described in Bormann, E. R. et al. (1992) Mol. Microbiol. 6: 317-326.

[0262] To assess the presence or relative quantity of protein translated from this mRNA, standard techniques, such as a Western blot, may be employed (see, for example, Ausubel et al. (1988) Current Protocols in Molecular Biology, Wiley: New York). In this process, total cellular proteins are extracted, separated by gel electrophoresis, transferred to a matrix such as nitrocellulose, and incubated with a probe, such as an antibody, which specifically binds to the desired protein. This probe is generally tagged with a chemiluminescent or colorimetric label which may be readily detected. The presence and quantity of label observed indicates the presence and quantity of the desired mutant protein present in the cell.

Example 15

[0263] Growth of Genetically Modified Corynebacterium Glutamicum—Media and Culture Conditions

[0264] Genetically modified Corynebacteria are cultured in synthetic or natural growth media. A number of different growth media for Corynebacteria are both well-known and readily available (Lieb et al. (1989) Appl. Microbiol. Biotechnol., 32:205-210; von der Osten et al. (1998) Biotechnology Letters, 11:11-16; Pat. DE 4,120,867; Liebl (1992) “The Genus Corynebacterium, in: The Procaryotes, Volume II, Balows, A. et al., eds. Springer-Verlag). These media consist of one or more carbon sources, nitrogen sources, inorganic salts, vitamins and trace elements. Preferred carbon sources are sugars, such as mono-, di-, or polysaccharides. For example, glucose, fructose, mannose, galactose, ribose, sorbose, ribulose, lactose, maltose, sucrose, raffmose, starch or cellulose serve as very good carbon sources. It is also possible to supply sugar to the media via complex compounds such as molasses or other by-products from sugar refinement. It can also be advantageous to supply mixtures of different carbon sources. Other possible carbon sources are alcohols and organic acids, such as methanol, ethanol, acetic acid or lactic acid. Nitrogen sources are usually organic or inorganic nitrogen compounds, or materials which contain these compounds. Exemplary nitrogen sources include ammonia gas or ammonia salts, such as NH₄Cl or (NH₄)₂SO₄, NH₄OH, nitrates, urea, amino acids or complex nitrogen sources like corn steep liquor, soy bean flour, soy bean protein, yeast extract, meat extract and others.

[0265] Inorganic salt compounds which may be included in the media include the chloride-, phosphorous- or sulfate-salts of calcium, magnesium, sodium, cobalt, molybdenum, potassium, manganese, zinc, copper and iron. Chelating compounds can be added to the medium to keep the metal ions in solution. Particularly useful chelating compounds include dihydroxyphenols, like catechol or protocatechuate, or organic acids, such as citric acid. It is typical for the media to also contain other growth factors, such as vitamins or growth promoters, examples of which include biotin, riboflavin, thiamin, folic acid, nicotinic acid, pantothenate and pyridoxin. Growth factors and salts frequently originate from complex media components such as yeast extract, molasses, corn steep liquor and others. The exact composition of the media compounds depends strongly on the immediate experiment and is individually decided for each specific case. Information about media optimization is available in the textbook “Applied Microbiol. Physiology, A Practical Approach (eds. P. M. Rhodes, P. F. Stanbury, IRL Press (1997) pp. 53-73, ISBN 0 19 963577 3). It is also possible to select growth media from commercial suppliers, like standard 1 (Merck) or BHI (grain heart infusion, DIFC) or others.

[0266] All medium components are sterilized, either by heat (20 minutes at 1.5 bar and 121□ C.) or by sterile filtration. The components can either be sterilized together or, if necessary, separately. All media components can be present at the beginning of growth, or they can optionally be added continuously or batchwise.

[0267] Culture conditions are defined separately for each experiment. The temperature should be in a range between 15□ C. and 45□ C. The temperature can be kept constant or can be altered during the experiment. The pH of the medium should be in the range of 5 to 8.5, preferably around 7.0, and can be maintained by the addition of buffers to the media. An exemplary buffer for this purpose is a potassium phosphate buffer. Synthetic buffers such as MOPS, HEPES, ACES and others can alternatively or simultaneously be used. It is also possible to maintain a constant culture pH through the addition of NaOH or NH₄OH during growth. If complex medium components such as yeast extract are utilized, the necessity for additional buffers may be reduced, due to the fact that many complex compounds have high buffer capacities. If a fermentor is utilized for culturing the micro-organisms, the pH can also be controlled using gaseous ammonia.

[0268] The incubation time is usually in a range from several hours to several days. This time is selected in order to permit the maximal amount of product to accumulate in the broth. The disclosed growth experiments can be carried out in a variety of vessels, such as microtiter plates, glass tubes, glass flasks or glass or metal fermentors of different sizes. For screening a large number of clones, the microorganisms should be cultured in microtiter plates, glass tubes or shake flasks, either with or without baffles. Preferably 100 ml shake flasks are used, filled with 10% (by volume) of the required growth medium. The flasks should be shaken on a rotary shaker (amplitude 25 mm) using a speed-range of 100-300 rpm. Evaporation losses can be diminished by the maintenance of a humid atmosphere; alternatively, a mathematical correction for evaporation losses should be performed.

[0269] If genetically modified clones are tested, an unmodified control clone or a control clone containing the basic plasmid without any insert should also be tested. The medium is inoculated to an OD₆₀₀ of 0.5-1.5 using cells grown on agar plates, such as CM plates (10 g/l glucose, 2,5 g/l NaCl, 2 g/l urea, 10 g/l polypeptone, 5 g/l yeast extract, 5 g/l meat extract, 22 g/l NaCl, 2 g/l urea, 10 g/l polypeptone, 5 g/l yeast extract, 5 g/l meat extract, 22 g/l agar, pH 6.8 with 2M NaOH) that had been incubated at 30□ C. Inoculation of the media is accomplished by either introduction of a saline suspension of C. glutamicum cells from CM plates or addition of a liquid preculture of this bacterium.

Example 16

[0270] In vitro Analysis of the Function of Physcomitrella Genes in Transgenic Organisms

[0271] The determination of activities and kinetic parameters of enzymes is well established in the art. Experiments to determine the activity of any given altered enzyme must be tailored to the specific activity of the wild-type enzyme, which is well within the ability of one skilled in the art. Overviews about enzymes in general, as well as specific details concerning structure, kinetics, principles, methods, applications and examples for the determination of many enzyme activities may be found, for example, in the following references: Dixon, M., and Webb, E. C., (1979) Enzymes. Longmans: London; Fersht, (1985) Enzyme Structure and Mechanism. Freeman: New York; Walsh, (1979) Enzymatic Reaction Mechanisms. Freeman: San Francisco; Price, N. C., Stevens, L. (1982) Fundamentals of Enzymology. Oxford Univ. Press: Oxford; Boyer, P. D., ed. (1983) The Enzymes, 3^(rd) ed. Academic Press: New York; Bisswanger, H., (1994) Enzymkinetik, 2^(nd) ed. VCH: Weinheim (ISBN 3527300325); Bergmeyer, H. U., Bergmeyer, J., Graβ1, M., eds. (1983-1986) Methods of Enzymatic Analysis, 3^(rd) ed., vol. I-XII, Verlag Chemie: Weinheim; and Ullmann's Encyclopedia of Industrial Chemistry (1987) vol. A9, “Enzymes”. VCH: Weinheim, p. 352-363.

[0272] The activity of proteins which bind to DNA can be measured by several well-established methods, such as DNA band-shift assays (also called gel retardation assays). The effect of such proteins on the expression of other molecules can be measured using reporter gene assays (such as that described in Kolmar, H. et al. (1995) EMBO J. 14: 3895-3904 and references cited therein). Reporter gene test systems are well known and established for applications in both pro- and eukaryotic cells, using enzymes such as beta-galactosidase, green fluorescent protein, and several others.

[0273] The determination of activity of membrane-transport proteins can be performed according to techniques such as those described in Gennis, R. B. (1989) “Pores, Channels and Transporters”, in Biomembranes, Molecular Structure and Function, Springer: Heidelberg, p. 85-137; 199-234; and 270-322.

Example 17

[0274] Analysis of Impact of Recombinant Proteins on the Production of the Desired Product

[0275] The effect of the genetic modification in plants, algae, C. glutamicum, fungi, cilates or on production of a desired compound (such as vitamins) can be assessed by growing the modified microorganism or plant under suitable conditions (such as those described above) and analyzing the medium and/or the cellular component for increased production of the desired product (i.e. fine chemicals). Such analysis techniques are well known to one skilled in the art, and include spectroscopy, thin layer chromatography, staining methods of various kinds, enzymatic and microbiological methods, and analytical chromatography such as high performance liquid chromatography (see, for example, Ullman, Encyclopedia of Industrial Chemistry, vol. A2, p. 89-90 and p. 443-613, VCH: Weinheim (1985); Fallon, A. et al., (1987) “Applications of HPLC in Biochemistry” in: Laboratory Techniques in Biochemistry and Molecular Biology, vol. 17; Rehm et al. (1993) Biotechnology, vol. 3, Chapter III: “Product recovery and purification”, page 469-714, VCH: Weinheim; Belter, P. A. et al. (1988) Bioseparations: downstream processing for biotechnology, John Wiley and Sons; Kennedy, J. F. and Cabral, J. M. S. (1992) Recovery processes for biological materials, John Wiley and Sons; Shaeiwitz, J. A. and Henry, J. D. (1988) Biochemical separations, in: Ulmann's Encyclopedia of Industrial Chemistry, vol. B3, Chapter 11, page 1-27, VCH: Weinheim; and Dechow, F. J. (1989) Separation and purification techniques in biotechnology, Noyes Publications.)

[0276] In addition to the measurement of the final product in plant cells, microorganisms and algae, it is also possible to analyze other components of the metabolic pathways utilized for the production of the desired compound, such as intermediates and side-products, to determine the overall efficiency of production of the compound. Analysis methods include measurements of nutrient levels in the medium (e.g., sugars, hydrocarbons, nitrogen sources, phosphate, and other ions), measurements of biomass composition and growth, analysis of the production of common metabolites of biosynthetic pathways, and measurement of gasses produced during fermentation. Standard methods for these measurements are outlined in Applied Microbial Physiology, A Practical Approach, P. M. Rhodes and P. F. Stanbury, eds., IRL Press, p. 103-129; 131-163; and 165-192 (ISBN: 0199635773) and references cited therein.

[0277] Material to be analyzed can be disintegrated via sonification, glass milling, liquid nitrogen and grinding or via other applicable methods. The material has to be centrifuged after disintegration.

[0278] Amino Acids

[0279] The determination of amino acids (except for proline) was performed as described in Geigenberger et al. (1996, Plant Cell & Environ. 19:43-55) using ethanolic extracts for HPLC analyses.

[0280] The concentration of proline was determined according to Bates et al. (1973, Plant Soil 39: 205-207).

[0281] Vitamin E

[0282] The determination of tocopherols in cells has been either conducted according to Kurilich et al 1999, J. Agric. Food. Chem. 47: 1576-1581 or alternatively as described in Tani Y and Tsumura H 1989 (Agric. Bio. Chem. 53: 305-312).

[0283] Carotenoids

[0284] The large scale production and purification of carotenoids implies a solution for separation of lipophilic impurities from the host cell which have to be separated from the carotenoids. On a production scale the material has to be desintegrated for the production of oleoresins via centrifugation as known skilled in the art from various production processes or via desintegration followed by evaporation and extraction. Acetone or hexane extraction for 8-12-hours in the dark to avoid carotenoid break down. After removal of the solvent the residue is dissolved in a diethylether-hexane mixture or, in case of hydroxycarotenoids, in acetone-petrol and purified via silica-gel column. Suitable solvent mixtures are diethylether:hexane or petrol (1:4 v/v) for carotenes and acetone:hexane or petrol (1:4 v/v) for hydroxycarotenoids. To determine carotenoid purity in isolated fractions HPLC techniques are most appropriate (Linden et al., FEMS Microbiol. Let. 106:99-104; Piccaglia et al., 1998; Industrial Crops and Products 8:45-51 and references therein).

[0285] Thiamin

[0286] For the determination of thiamin in plants, in micro-organisms or in other substances, physicochemical and microbiolagical methods are employed (Al-Rashood et al., Anal. Profiles Drug Subst.18, 1989, 414).

[0287] For complex biological materials treatments or purification may be necessary to remove compound which might interfere with the analyses.

[0288] The flourometric method is based on the oxidation of thiamin to thiochrome by an alkaline solution of potassium ferricyanide. The tiochrome is extracted into isobutanol and the fluorescence of the extract at an emission wavelength of 436 mn compared with that of standard thiochrome solution.

[0289] Thiamin can be also determined sprectrophotometrically by measuring its UV absorption 266 nm, but only in cases were no other materials absorbing at this wavelength are present in significant amounts.

[0290] Microbiologically assays are simple, inexpensive and quite sensitive (detection limit 5-50 ng thiamin), but their main drawback is the longer period of time to obtain the results (Friedrich, Urban &Schwarzenberg, Handbuch der Vitamine1987).

[0291] Riboflavin

[0292] Several Methods for detection of Riboflavin from living sources have been described (Friedrich, W. Vitamins, De Gruyter, 1988 and references therein). In the lumiflavin method, riboflavin is converted to lumiflavin by irradiation, which can be extracted by trichloromethane and measured either photometrically at 450 nm or fluorometrically at 513 nm. Interference with accompanying substances with similar fluorescence can be eliminated by quenching the fluorescence of riboflavin with Na₂S₂O₄ (Strohecker and Henning, “Vitaminbestimmungen”, Verlag Chemie, Weinheim, 1963, pp. 101ff). After extraction in suitable buffer systems determination of Riboflavin as well as FAD and FMN from plants and microorganisms have been most practically and automatically performed by reversed phase HPLC-analysis as described (Lumley et al., Analyst 106, 1103 ff. 1981).

[0293] Vitamin C

[0294] Several Methods for detection of vitamin C from living sources have been described (Friedrich, W. Vitamins, De Gruyter, 1988 and references therein). After extraction in suitable buffer systems determination of vitamin C from plants and microorganisms have been most practically and automatically performed by reversed phase HPLC-method with post column oxidation/reduction system in conjunction with UV-, electrochemical- or fluorometric detection of ascorbic acid (Uliman's Encyclopedia of Industrial Chemistry, “Vitamins” vol. A27, p. 550, VCH: Weinheim, 1996 and references therein).

[0295] Vitamin B6

[0296] Several Methods for detection of panothenate from living sources have been described like use of microorganisms, enzmatic tests, immunological assays, gaschromatographic and HPLC methods. (Friedrich, W. Vitamins, De Gruyter, 1988 and references therein). After extraction in suitable buffer systems determination of vitamin C from plants, microorganisms and algae are most practically and automatically performed by a reversed phase HPLC-method as described (Williams, Methods in Enzymology 62, pp 415-22, 1979).

[0297] Panthotenate

[0298] Several Methods for detection of panothenate from living sources have been described like radioimmunoassays, immunological ELISAs, gaschromatographic and HPLC methods and enzymatic tests. (Friedrich, W. Vitamins, De Gruyter, 1988 and references therein). After extraction in suitable buffer systems determination of pantothenate from plants and microorganisms are most practically and automatically performed by reversed phase HPLC-analysis according to Jonvel et al. Chromatographie 281, PP 371ff, 1983.

[0299] Niacin

[0300] Assays of the pure substances are most readily determined by titration. Nicotinic acid is determined by titration with sodium hydroxide or UV spectoscopy (United States Pharmacopoeia, vol. 23, USP Convention, Inc. Princeton, N.J. 1990, p. 1080). Nicotinamid is determined by titration with perchloric acid in acetic acid or UV spectroscopy. For assays in biological material microbiological, spectrophotometric and chromatografic procedures are described for quantitative determination of nicotinic acid or nicotinamide (Helrich, Association of Analytical Chemists: Official Methods of Analysis, 15th ed. Arlington, Va. 1990, Microbiology, 960.46 and 985.43).

[0301] Nucleotides

[0302] The determination of nucleotides was performed as described in Stitt et al., FEBS Letters 145(1982), 217-222.

Example 18

[0303] Purification of the Desired Product from Transformed Organisms

[0304] Recovery of the desired product from plants material or fungi, algae, cilates or C. glutamicum cells or supernatant of the above-described cultures can be performed by various methods well known in the art. If the desired product is not secreted from the cells. The cells, can be harvested from the culture by low-speed centrifugation, the cells can be lysed by standard techniques, such as mechanical force or sonification. Organs of plants can be separated mechanically from other tissue or organs. Following homogenization cellular debris is removed by centrifugation, and the supernatant fraction containing the soluble proteins is retained for further purification of the desired compound. If the product is secreted from desired cells, then the cells are removed from the culture by low-speed centrifugation, and the supernate fraction is retained for further purification.

[0305] The supernatant fraction from either purification method is subjected to chromatography with a suitable resin, in which the desired molecule is either retained on a chromatography resin while many of the impurities in the sample are not, or where the impurities are retained by the resin while the sample is not. Such chromatography steps may be repeated as necessary, using the same or different chromatography resins. One skilled in the art would be well-versed in the selection of appropriate chromatography resins and in their most efficacious application for a particular molecule to be purified. The purified product may be concentrated by filtration or ultrafiltration, and stored at a temperature at which the stability of the product is maximized.

[0306] There are a wide array of purification methods known to the art and the preceding method of purification is not meant to be limiting. Such purification techniques are described, for example, in Bailey, J. E. & Ollis, D. F. Biochemical Engineering Fundamentals, McGraw-Hill: New York (1986).

[0307] The identity and purity of the isolated compounds may be assessed by techniques standard in the art. These include high-performance liquid chromatography (HPLC), spectroscopic methods, staining methods, thin layer chromatography, NIRS, enzymatic assay, or microbiologically. Such analysis methods are reviewed in: Patek et al. (1994) Appl. Environ. Microbiol. 60: 133-140; Malakhova et al. (1996) Biotekhnologiya 11: 27-32; and Schmidt et al. (1998) Bioprocess Engineer. 19: 67-70. Ulmann's Encyclopedia of Industrial Chemistry, (1996) vol. A27, VCH: Weinheim, p. 89-90, p. 521-540, p. 540-547, p. 559-566, 575-581 and p. 581-587; Michal, G. (1999) Biochemical Pathways: An Atlas of Biochemistry and Molecular Biology, John Wiley and Sons; Fallon, A. et al. (1987) Applications of HPLC in Biochemistry in: Laboratory Techniques in Biochemistry and Molecular Biology, vol. 17.

[0308] Equivalents

[0309] Those skilled in the art will recognize, or will be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. Such equivalents are intended to be encompassed by the following claims. TABLE 1 Start Stop of open of open Function/Amino reading reading acid metabolism Acc. no./Entry no. frame frame Leucine, valine metabolism Acetolactate Synthase 63_ck26_c05fwd 1-3 514-516 Ketol-Acid 24_ppprot1_087_d09 1-3 484-486 Reductoisomerase Ketol-Acid 07_ppprot1_061_b01 3-5 321-323 Reductoisomerase Ketol-Acid 30_mm1_e09rev 3-5 567-569 Reductoisomerase Leucin/Glutamate 42_ck9_g09fwd 2-4 461-463 Dehydrogenase Isopropylmalate 52_ppprot1_50_a11 2-4 605-607 Isomerase (large subunit) Tryptophan metabolism Trypthophan Synthase 83_ppprot1_075_f06 3-5 507-509 (alpha-chain) Trypthophan Synthase 76_mm2_e11rev 2-4 641-643 (alpha-chain) Histidine metabolism ATP Phosphoribosyl- 94_ppprot3_001_h11 2-4 401-403 transferase Lysine, methionine, Isoleucine metabolism Dihydrodipicolinate 11_ppprot1_096_b03 185-187 401-403 Synthase Methionine Synthase 34_ppprot3_002_f08 1-3 613-615 Cysteine Synthase B 94_ppprot1_072_h11 3-5 606-608 Cysteine Synthase B 02_ck18_a07fwd 2-4 353-355 Cysteine Synthase B 72ck11_d12fwd 1-3 490-492 Nitrate Reductase 41_ppprot1_054_g03 1-3 517-519 Nitrate Reductase 54_ppprot3_002_a12 2-4 551-553 Riboflavin metabolism Riboflavin Synthase 71_ppprot1_60_d06 114-116 528-530 Riboflavin Synthase 32_ck1_f07fwd 3-5 321-323 acid phosphatase 78_ck8_e12fwd 2-4 500-502 nucleotid 25_ppprot1_098_e01 1-3 289-291 pyrophosphatase Pantothenate metabolism branched-chain amino 35_ppprot1_099_f03 1-3 535-537 acid transaminase 3-methyl-2- 85_bd02_g04rev 3-5 558-580 oxobutanoate hydroxy- methyl-transferase Vitamin B6 metabolism class v pyridoxal 85_ppprot1_083_g04 2-4 145-547 phosphate dependent aminotransferase threonine synthase 45_ppprot1_093_h02 274-276 634-636 Vitamin C metabolism Phosphomannomutase 42_ppprot1 3-5 489-491 GDP-mannose 05_ck3_a03fwd 161-163 329-331 pyrophosphorylase Ascorbat peroxidase 56_ppprot1_105_b10 52-54 577-579 Thiamin metabolism thiamine biosynthetic 87_ppprot135_g05 1-3 364-366 enzyme (thi 1-2) thiazole biosynthetic 47_mm13_h03rev 1-3 376-378 enzyme Folate metabolism formate tetra- 47_ppprot1_093_h03 2-4 263-265 hydrofolate ligase methylenetetra- 86_ppprot1_094_g10 1-3 571-573 hydrofolate reductase methylenetetra- 62_mm20_c10rev 2-4 407-409 hydrofolate reductase polyglutamate 22_ck26_d08fwd 3-5 447-449 synthetase Nucleotide metabolism mitochondrial 5_ck15_b10fwd 74-76 491-493 ATP/ADP carrier UMP Synthase (de- 11_mm6 3-5 531-533 carboxylase domain) inosine-uridine 13_ck25_c01fwd 33-35 474-476 preferring nucleoside hydrolase glycinamide 42_ppprot1_075_g09 2-4 581-583 ribonucleotide transformylase IMP dehydrogenase 44_ppprot3_003_h07 2-4 467-469 adenylosuccinate 84_ppprot3_001_f12 1-3 550-552 synthase phosphodiesterase 77_ck14_e06fwd 263-265 536-538 cytosolic IMP-GMP 17_ck3_c03fwd 2-4 287-289 specific 5′-nucleotidase uricase 44_ck20_h07fwd 1-3 514-516

[0310]

1 87 1 518 DNA Physcomitrella patens CDS (1)..(516) 63_ck26_c05fwd 1 ctg aaa ccc aac gcc agc gaa agc att gtg gtc gcc ttg ggt gct gca 48 Leu Lys Pro Asn Ala Ser Glu Ser Ile Val Val Ala Leu Gly Ala Ala 1 5 10 15 aca act atg gcc atg atg gcg gag gtg atg gct cga ggg agt tcg aca 96 Thr Thr Met Ala Met Met Ala Glu Val Met Ala Arg Gly Ser Ser Thr 20 25 30 ttg ctc ggt tct gcc tcg tct gtc gtc gtt cct tgc aaa aag gcg ccg 144 Leu Leu Gly Ser Ala Ser Ser Val Val Val Pro Cys Lys Lys Ala Pro 35 40 45 gca acg cct ttc tta ggt gcc tca tta ccc tca ctc tcg acg ggc gca 192 Ala Thr Pro Phe Leu Gly Ala Ser Leu Pro Ser Leu Ser Thr Gly Ala 50 55 60 cgc aag aac aaa cct caa tgc aac ctt gca gtg agc gca acc aag gct 240 Arg Lys Asn Lys Pro Gln Cys Asn Leu Ala Val Ser Ala Thr Lys Ala 65 70 75 80 agc ctg agc gat gct ctg agc aag gcc aaa tcc act gtg ggc act ggg 288 Ser Leu Ser Asp Ala Leu Ser Lys Ala Lys Ser Thr Val Gly Thr Gly 85 90 95 ctg gcc gcc ttg gcc ctc tcc gcg gcg atg aac ctc tgc cca gca gtc 336 Leu Ala Ala Leu Ala Leu Ser Ala Ala Met Asn Leu Cys Pro Ala Val 100 105 110 ccc tac tcg gaa gcc agc gag ttc aac gtc ttg aac gaa ggc ccg ccc 384 Pro Tyr Ser Glu Ala Ser Glu Phe Asn Val Leu Asn Glu Gly Pro Pro 115 120 125 acg gaa aac ttc gtg gta gat gat gcc aac gtg ctc aac cgc gtc aca 432 Thr Glu Asn Phe Val Val Asp Asp Ala Asn Val Leu Asn Arg Val Thr 130 135 140 aaa tct gac ata aag cgc ttg ctt cgt gac ctc gaa gag cgc aag ggc 480 Lys Ser Asp Ile Lys Arg Leu Leu Arg Asp Leu Glu Glu Arg Lys Gly 145 150 155 160 tac cac att aac gtc atc act ctt gag gaa gct tca ct 518 Tyr His Ile Asn Val Ile Thr Leu Glu Glu Ala Ser 165 170 2 172 PRT Physcomitrella patens 2 Leu Lys Pro Asn Ala Ser Glu Ser Ile Val Val Ala Leu Gly Ala Ala 1 5 10 15 Thr Thr Met Ala Met Met Ala Glu Val Met Ala Arg Gly Ser Ser Thr 20 25 30 Leu Leu Gly Ser Ala Ser Ser Val Val Val Pro Cys Lys Lys Ala Pro 35 40 45 Ala Thr Pro Phe Leu Gly Ala Ser Leu Pro Ser Leu Ser Thr Gly Ala 50 55 60 Arg Lys Asn Lys Pro Gln Cys Asn Leu Ala Val Ser Ala Thr Lys Ala 65 70 75 80 Ser Leu Ser Asp Ala Leu Ser Lys Ala Lys Ser Thr Val Gly Thr Gly 85 90 95 Leu Ala Ala Leu Ala Leu Ser Ala Ala Met Asn Leu Cys Pro Ala Val 100 105 110 Pro Tyr Ser Glu Ala Ser Glu Phe Asn Val Leu Asn Glu Gly Pro Pro 115 120 125 Thr Glu Asn Phe Val Val Asp Asp Ala Asn Val Leu Asn Arg Val Thr 130 135 140 Lys Ser Asp Ile Lys Arg Leu Leu Arg Asp Leu Glu Glu Arg Lys Gly 145 150 155 160 Tyr His Ile Asn Val Ile Thr Leu Glu Glu Ala Ser 165 170 3 488 DNA Physcomitrella patens CDS (1)..(486) 24_ppprot1_087_d09 3 gtt cgc atc cct ccg ctc tgt tgt gga ggc cct gct ctc ctc ctc tcc 48 Val Arg Ile Pro Pro Leu Cys Cys Gly Gly Pro Ala Leu Leu Leu Ser 1 5 10 15 cca ttc ctg gtc cct cgt cct cct tct gta gag cgc gag tgt gtg tgt 96 Pro Phe Leu Val Pro Arg Pro Pro Ser Val Glu Arg Glu Cys Val Cys 20 25 30 gtg tgt tat cca ggg ctt tcc acc atg gcc gct gtt act ctc tcc cac 144 Val Cys Tyr Pro Gly Leu Ser Thr Met Ala Ala Val Thr Leu Ser His 35 40 45 tgt gcc gca ccc tcc tca tct gtg gca cac cgc tcc tcc gag gtg ctg 192 Cys Ala Ala Pro Ser Ser Ser Val Ala His Arg Ser Ser Glu Val Leu 50 55 60 ggt agc gct ggc ccc aag atg acc tcc ttc gca ggg ttg agg tct gtg 240 Gly Ser Ala Gly Pro Lys Met Thr Ser Phe Ala Gly Leu Arg Ser Val 65 70 75 80 gcg ttc gct ccc aaa ctt gag aag agc ttg agg aat gct gtg gcc gcc 288 Ala Phe Ala Pro Lys Leu Glu Lys Ser Leu Arg Asn Ala Val Ala Ala 85 90 95 gtg cct tgc tgg cgg cgg ggc ggt gct atg tct atc aac atg gtg gct 336 Val Pro Cys Trp Arg Arg Gly Gly Ala Met Ser Ile Asn Met Val Ala 100 105 110 aca cct gct gtg cgt ggt gtc gat gtg gag ttt cag act gag atc ttt 384 Thr Pro Ala Val Arg Gly Val Asp Val Glu Phe Gln Thr Glu Ile Phe 115 120 125 aag aag gaa aag att acc cct gcc ggc cgt gat gag tac att gtc cga 432 Lys Lys Glu Lys Ile Thr Pro Ala Gly Arg Asp Glu Tyr Ile Val Arg 130 135 140 ggt gga cgg gac ctg ttc cat ttg ctg ccg aag gct ctt aca ggg atc 480 Gly Gly Arg Asp Leu Phe His Leu Leu Pro Lys Ala Leu Thr Gly Ile 145 150 155 160 aag aaa at 488 Lys Lys 4 162 PRT Physcomitrella patens 4 Val Arg Ile Pro Pro Leu Cys Cys Gly Gly Pro Ala Leu Leu Leu Ser 1 5 10 15 Pro Phe Leu Val Pro Arg Pro Pro Ser Val Glu Arg Glu Cys Val Cys 20 25 30 Val Cys Tyr Pro Gly Leu Ser Thr Met Ala Ala Val Thr Leu Ser His 35 40 45 Cys Ala Ala Pro Ser Ser Ser Val Ala His Arg Ser Ser Glu Val Leu 50 55 60 Gly Ser Ala Gly Pro Lys Met Thr Ser Phe Ala Gly Leu Arg Ser Val 65 70 75 80 Ala Phe Ala Pro Lys Leu Glu Lys Ser Leu Arg Asn Ala Val Ala Ala 85 90 95 Val Pro Cys Trp Arg Arg Gly Gly Ala Met Ser Ile Asn Met Val Ala 100 105 110 Thr Pro Ala Val Arg Gly Val Asp Val Glu Phe Gln Thr Glu Ile Phe 115 120 125 Lys Lys Glu Lys Ile Thr Pro Ala Gly Arg Asp Glu Tyr Ile Val Arg 130 135 140 Gly Gly Arg Asp Leu Phe His Leu Leu Pro Lys Ala Leu Thr Gly Ile 145 150 155 160 Lys Lys 5 487 DNA Physcomitrella patens CDS (3)..(323) 07_ppprot1_061_b01 5 cg gag atg gtt aac gaa agt gtg att gag gct gtt gac tct ctc aac 47 Glu Met Val Asn Glu Ser Val Ile Glu Ala Val Asp Ser Leu Asn 1 5 10 15 cct ttc atg cac gcc cgt ggt gta gcc ttc atg gtg gac aac tgc tca 95 Pro Phe Met His Ala Arg Gly Val Ala Phe Met Val Asp Asn Cys Ser 20 25 30 aca act gct cgt ctc ggt tcc cgc aaa tgg gcg cca cga ttt gat tac 143 Thr Thr Ala Arg Leu Gly Ser Arg Lys Trp Ala Pro Arg Phe Asp Tyr 35 40 45 att ttg act cag cag gct tac acc gca gta gat aac gga act ccc att 191 Ile Leu Thr Gln Gln Ala Tyr Thr Ala Val Asp Asn Gly Thr Pro Ile 50 55 60 aac aag gat gtt cta gag agc ttc agg gca gac ccg gtt cac cag gcc 239 Asn Lys Asp Val Leu Glu Ser Phe Arg Ala Asp Pro Val His Gln Ala 65 70 75 atc gct gtc tgc gca gaa ttg agg ccc agt gtt gat att gct gta gct 287 Ile Ala Val Cys Ala Glu Leu Arg Pro Ser Val Asp Ile Ala Val Ala 80 85 90 95 gag gat gct gac tac gtc aga gct gaa tta cga caa tagagggacg 333 Glu Asp Ala Asp Tyr Val Arg Ala Glu Leu Arg Gln 100 105 gtttctggcc caacgtagat gattatttta ccttaaggtc ctagaccaca gaggttttaa 393 aatgggcttg gaggtttatt tgtggaggat gaattgattg ttcctcatan atgtgcctcc 453 acaagcgaat gaatgcgttc acgatcatgg tttt 487 6 107 PRT Physcomitrella patens 6 Glu Met Val Asn Glu Ser Val Ile Glu Ala Val Asp Ser Leu Asn Pro 1 5 10 15 Phe Met His Ala Arg Gly Val Ala Phe Met Val Asp Asn Cys Ser Thr 20 25 30 Thr Ala Arg Leu Gly Ser Arg Lys Trp Ala Pro Arg Phe Asp Tyr Ile 35 40 45 Leu Thr Gln Gln Ala Tyr Thr Ala Val Asp Asn Gly Thr Pro Ile Asn 50 55 60 Lys Asp Val Leu Glu Ser Phe Arg Ala Asp Pro Val His Gln Ala Ile 65 70 75 80 Ala Val Cys Ala Glu Leu Arg Pro Ser Val Asp Ile Ala Val Ala Glu 85 90 95 Asp Ala Asp Tyr Val Arg Ala Glu Leu Arg Gln 100 105 7 570 DNA Physcomitrella patens CDS (3)..(569) 30_mm1_e09rev 7 tt cca cag gaa aca gct atg acc atg att acg cca agc tcg aaa tta 47 Pro Gln Glu Thr Ala Met Thr Met Ile Thr Pro Ser Ser Lys Leu 1 5 10 15 acc ctc act aaa ggg aac aaa agc tgg agc tcc acc gcg gtg gcg gcc 95 Thr Leu Thr Lys Gly Asn Lys Ser Trp Ser Ser Thr Ala Val Ala Ala 20 25 30 gct cta gaa cta gtg gat ccc ccg ggc tgc agg aat tcg gca cca gga 143 Ala Leu Glu Leu Val Asp Pro Pro Gly Cys Arg Asn Ser Ala Pro Gly 35 40 45 gct gtg cac ggt ata gta gaa tct ttg ttc agg cgg tac act gcc cag 191 Ala Val His Gly Ile Val Glu Ser Leu Phe Arg Arg Tyr Thr Ala Gln 50 55 60 ggt atg tct gaa gag gat gct tac aag aac act gtg gag ggc atc act 239 Gly Met Ser Glu Glu Asp Ala Tyr Lys Asn Thr Val Glu Gly Ile Thr 65 70 75 ggc gtc atc tcc aaa atc att tca act aag ggc att ttg gct gtt tac 287 Gly Val Ile Ser Lys Ile Ile Ser Thr Lys Gly Ile Leu Ala Val Tyr 80 85 90 95 gag gct tta agt gag gaa ggt aag aag gag ttt gag gca gcc tac agc 335 Glu Ala Leu Ser Glu Glu Gly Lys Lys Glu Phe Glu Ala Ala Tyr Ser 100 105 110 gct tct ttc tac ccc tct atg gat atc ctc tat gag tgc tac gag gat 383 Ala Ser Phe Tyr Pro Ser Met Asp Ile Leu Tyr Glu Cys Tyr Glu Asp 115 120 125 gtt gct tcc ggt aat gag atc cgc agc gtc gta ctg gct ggt cgc aga 431 Val Ala Ser Gly Asn Glu Ile Arg Ser Val Val Leu Ala Gly Arg Arg 130 135 140 ttt tcc gag aaa gag ggt ctg cca gct ttt cct atg ggg aag atc gat 479 Phe Ser Glu Lys Glu Gly Leu Pro Ala Phe Pro Met Gly Lys Ile Asp 145 150 155 gga acc cgc atg tgg caa gtt ggt gag aaa gtt cgg gct tca cga ccc 527 Gly Thr Arg Met Trp Gln Val Gly Glu Lys Val Arg Ala Ser Arg Pro 160 165 170 175 aag ggt gac atg ggt cca ctc cac cca ttc act gcc ggt gta t 570 Lys Gly Asp Met Gly Pro Leu His Pro Phe Thr Ala Gly Val 180 185 8 189 PRT Physcomitrella patens 8 Pro Gln Glu Thr Ala Met Thr Met Ile Thr Pro Ser Ser Lys Leu Thr 1 5 10 15 Leu Thr Lys Gly Asn Lys Ser Trp Ser Ser Thr Ala Val Ala Ala Ala 20 25 30 Leu Glu Leu Val Asp Pro Pro Gly Cys Arg Asn Ser Ala Pro Gly Ala 35 40 45 Val His Gly Ile Val Glu Ser Leu Phe Arg Arg Tyr Thr Ala Gln Gly 50 55 60 Met Ser Glu Glu Asp Ala Tyr Lys Asn Thr Val Glu Gly Ile Thr Gly 65 70 75 80 Val Ile Ser Lys Ile Ile Ser Thr Lys Gly Ile Leu Ala Val Tyr Glu 85 90 95 Ala Leu Ser Glu Glu Gly Lys Lys Glu Phe Glu Ala Ala Tyr Ser Ala 100 105 110 Ser Phe Tyr Pro Ser Met Asp Ile Leu Tyr Glu Cys Tyr Glu Asp Val 115 120 125 Ala Ser Gly Asn Glu Ile Arg Ser Val Val Leu Ala Gly Arg Arg Phe 130 135 140 Ser Glu Lys Glu Gly Leu Pro Ala Phe Pro Met Gly Lys Ile Asp Gly 145 150 155 160 Thr Arg Met Trp Gln Val Gly Glu Lys Val Arg Ala Ser Arg Pro Lys 165 170 175 Gly Asp Met Gly Pro Leu His Pro Phe Thr Ala Gly Val 180 185 9 463 DNA Physcomitrella patens CDS (2)..(463) 42_ck9_g09fwd 9 c cgg gat tta agt cca acc gaa ctt gaa cga tta acg cga gtg ttc acg 49 Arg Asp Leu Ser Pro Thr Glu Leu Glu Arg Leu Thr Arg Val Phe Thr 1 5 10 15 cag aag atc cat gat gtc atc ggt cct cat ctt gac atc cca gcc ccg 97 Gln Lys Ile His Asp Val Ile Gly Pro His Leu Asp Ile Pro Ala Pro 20 25 30 gac atg ggt acc aat gct cag act atg gct tgg att ttg gac gag tac 145 Asp Met Gly Thr Asn Ala Gln Thr Met Ala Trp Ile Leu Asp Glu Tyr 35 40 45 tcg aaa ttt cat ggg tat act ccg gcc gtc gta act ggt aaa ccg gtg 193 Ser Lys Phe His Gly Tyr Thr Pro Ala Val Val Thr Gly Lys Pro Val 50 55 60 gac ttg gga ggg tct ctt ggg cgg gaa gct gcc act gga aga ggt gtg 241 Asp Leu Gly Gly Ser Leu Gly Arg Glu Ala Ala Thr Gly Arg Gly Val 65 70 75 80 cta tat gca aca gag gct ctg ctt aag gat cat aac ctc agc att agg 289 Leu Tyr Ala Thr Glu Ala Leu Leu Lys Asp His Asn Leu Ser Ile Arg 85 90 95 ggc caa acg ttc gtt gtc caa ggc ttt ggg aat gtg ggt tct tgg gca 337 Gly Gln Thr Phe Val Val Gln Gly Phe Gly Asn Val Gly Ser Trp Ala 100 105 110 tcg aaa ctt atc cac gaa aag ggt gga aaa att aag gct gtt agt gat 385 Ser Lys Leu Ile His Glu Lys Gly Gly Lys Ile Lys Ala Val Ser Asp 115 120 125 gtt act gga gcc atc aag aac aac tct ggc att gat ata acc gcg ctt 433 Val Thr Gly Ala Ile Lys Asn Asn Ser Gly Ile Asp Ile Thr Ala Leu 130 135 140 aat gaa cac gtg cgg atg acc gga gga gtc 463 Asn Glu His Val Arg Met Thr Gly Gly Val 145 150 10 154 PRT Physcomitrella patens 10 Arg Asp Leu Ser Pro Thr Glu Leu Glu Arg Leu Thr Arg Val Phe Thr 1 5 10 15 Gln Lys Ile His Asp Val Ile Gly Pro His Leu Asp Ile Pro Ala Pro 20 25 30 Asp Met Gly Thr Asn Ala Gln Thr Met Ala Trp Ile Leu Asp Glu Tyr 35 40 45 Ser Lys Phe His Gly Tyr Thr Pro Ala Val Val Thr Gly Lys Pro Val 50 55 60 Asp Leu Gly Gly Ser Leu Gly Arg Glu Ala Ala Thr Gly Arg Gly Val 65 70 75 80 Leu Tyr Ala Thr Glu Ala Leu Leu Lys Asp His Asn Leu Ser Ile Arg 85 90 95 Gly Gln Thr Phe Val Val Gln Gly Phe Gly Asn Val Gly Ser Trp Ala 100 105 110 Ser Lys Leu Ile His Glu Lys Gly Gly Lys Ile Lys Ala Val Ser Asp 115 120 125 Val Thr Gly Ala Ile Lys Asn Asn Ser Gly Ile Asp Ile Thr Ala Leu 130 135 140 Asn Glu His Val Arg Met Thr Gly Gly Val 145 150 11 607 DNA Physcomitrella patens CDS (2)..(607) 52_ppprot1_50_a11 11 g tta gcc aag gat ctc ata ttg cag att atc ggt gaa ata tct gtt gca 49 Leu Ala Lys Asp Leu Ile Leu Gln Ile Ile Gly Glu Ile Ser Val Ala 1 5 10 15 ggg gca act tac aga gcg atg gag ttt gtc ggc act gcc gtt gat gct 97 Gly Ala Thr Tyr Arg Ala Met Glu Phe Val Gly Thr Ala Val Asp Ala 20 25 30 atg acg atg gaa gac aga atg act ctg tgc aac atg gtc gtg gaa gct 145 Met Thr Met Glu Asp Arg Met Thr Leu Cys Asn Met Val Val Glu Ala 35 40 45 gga ggc aag aat ggc gtt gtt cct gct gat gcc aca acc gcg aag tac 193 Gly Gly Lys Asn Gly Val Val Pro Ala Asp Ala Thr Thr Ala Lys Tyr 50 55 60 ttg gaa gga aaa acc tca aaa ccg tat caa gtt ttc act agt gat gga 241 Leu Glu Gly Lys Thr Ser Lys Pro Tyr Gln Val Phe Thr Ser Asp Gly 65 70 75 80 aac gcc agc ttc tta caa gaa tac aga ttt gac gtc tca aag ctg gag 289 Asn Ala Ser Phe Leu Gln Glu Tyr Arg Phe Asp Val Ser Lys Leu Glu 85 90 95 cct ctt gta gcc aag cca cat tct cca gac aac agg ggt ttg gct cga 337 Pro Leu Val Ala Lys Pro His Ser Pro Asp Asn Arg Gly Leu Ala Arg 100 105 110 gag tgc aag gat gtt aag att gac cgc gtt tac att ggg tca tgc act 385 Glu Cys Lys Asp Val Lys Ile Asp Arg Val Tyr Ile Gly Ser Cys Thr 115 120 125 ggt gga aag act gaa gat ttc ctt gct gct gca gag ctt ctg gca atc 433 Gly Gly Lys Thr Glu Asp Phe Leu Ala Ala Ala Glu Leu Leu Ala Ile 130 135 140 tca ggt caa aaa gtg aag gtg cca aca ttc ctt gtg cct gct aca cag 481 Ser Gly Gln Lys Val Lys Val Pro Thr Phe Leu Val Pro Ala Thr Gln 145 150 155 160 aag gtc tgg atg gac ttg tac tct ctg cca gta cct gga act gat gga 529 Lys Val Trp Met Asp Leu Tyr Ser Leu Pro Val Pro Gly Thr Asp Gly 165 170 175 aag acg tgt gcg gaa atc ttt cag caa gca ggt tgt gat act cct gct 577 Lys Thr Cys Ala Glu Ile Phe Gln Gln Ala Gly Cys Asp Thr Pro Ala 180 185 190 tct ccc tcg tgt gct gct tgc ctg ggt ggc 607 Ser Pro Ser Cys Ala Ala Cys Leu Gly Gly 195 200 12 202 PRT Physcomitrella patens 12 Leu Ala Lys Asp Leu Ile Leu Gln Ile Ile Gly Glu Ile Ser Val Ala 1 5 10 15 Gly Ala Thr Tyr Arg Ala Met Glu Phe Val Gly Thr Ala Val Asp Ala 20 25 30 Met Thr Met Glu Asp Arg Met Thr Leu Cys Asn Met Val Val Glu Ala 35 40 45 Gly Gly Lys Asn Gly Val Val Pro Ala Asp Ala Thr Thr Ala Lys Tyr 50 55 60 Leu Glu Gly Lys Thr Ser Lys Pro Tyr Gln Val Phe Thr Ser Asp Gly 65 70 75 80 Asn Ala Ser Phe Leu Gln Glu Tyr Arg Phe Asp Val Ser Lys Leu Glu 85 90 95 Pro Leu Val Ala Lys Pro His Ser Pro Asp Asn Arg Gly Leu Ala Arg 100 105 110 Glu Cys Lys Asp Val Lys Ile Asp Arg Val Tyr Ile Gly Ser Cys Thr 115 120 125 Gly Gly Lys Thr Glu Asp Phe Leu Ala Ala Ala Glu Leu Leu Ala Ile 130 135 140 Ser Gly Gln Lys Val Lys Val Pro Thr Phe Leu Val Pro Ala Thr Gln 145 150 155 160 Lys Val Trp Met Asp Leu Tyr Ser Leu Pro Val Pro Gly Thr Asp Gly 165 170 175 Lys Thr Cys Ala Glu Ile Phe Gln Gln Ala Gly Cys Asp Thr Pro Ala 180 185 190 Ser Pro Ser Cys Ala Ala Cys Leu Gly Gly 195 200 13 511 DNA Physcomitrella patens CDS (3)..(509) 83_ppprot1_075_f06 13 gc tgc tgc cag tgc cta ttt cac gct ccc gga aca gac gcg cat ttt 47 Cys Cys Gln Cys Leu Phe His Ala Pro Gly Thr Asp Ala His Phe 1 5 10 15 tct gca ata gct atg gcg ctt gtt agg gga cct atc gga gta gca acc 95 Ser Ala Ile Ala Met Ala Leu Val Arg Gly Pro Ile Gly Val Ala Thr 20 25 30 gtc ggc tcg tct ggg aaa gcg cgg ctg cag gat gca gtg gcg tct caa 143 Val Gly Ser Ser Gly Lys Ala Arg Leu Gln Asp Ala Val Ala Ser Gln 35 40 45 ttc gcc gcg cgt acc acg tgc tta cca tcc ctg gtg tcg ctg aac cac 191 Phe Ala Ala Arg Thr Thr Cys Leu Pro Ser Leu Val Ser Leu Asn His 50 55 60 ttt cct tcg caa ttc tgc gtt tcc tcc tgt gag ggt gct cgt tgt tca 239 Phe Pro Ser Gln Phe Cys Val Ser Ser Cys Glu Gly Ala Arg Cys Ser 65 70 75 agt gca tct aag cag cga cct gtg atg ccc cga gct act gcc gct cac 287 Ser Ala Ser Lys Gln Arg Pro Val Met Pro Arg Ala Thr Ala Ala His 80 85 90 95 gcc tca aac act cag agc atg act aga att gct gac aca ttt tct aca 335 Ala Ser Asn Thr Gln Ser Met Thr Arg Ile Ala Asp Thr Phe Ser Thr 100 105 110 ctt aag cag cta gga aag gtg gcc ttc att cca tac tta act gcc ggc 383 Leu Lys Gln Leu Gly Lys Val Ala Phe Ile Pro Tyr Leu Thr Ala Gly 115 120 125 gac cct gac ttg gat aca acg gct cag gca tta cgt cta ctg gat gac 431 Asp Pro Asp Leu Asp Thr Thr Ala Gln Ala Leu Arg Leu Leu Asp Asp 130 135 140 tgt gga gca gac atc ata gag ctt gga gtt ccc tac tca gat cct ctt 479 Cys Gly Ala Asp Ile Ile Glu Leu Gly Val Pro Tyr Ser Asp Pro Leu 145 150 155 gct gat ggc cct gtc att cag gct gcc gca ac 511 Ala Asp Gly Pro Val Ile Gln Ala Ala Ala 160 165 14 169 PRT Physcomitrella patens 14 Cys Cys Gln Cys Leu Phe His Ala Pro Gly Thr Asp Ala His Phe Ser 1 5 10 15 Ala Ile Ala Met Ala Leu Val Arg Gly Pro Ile Gly Val Ala Thr Val 20 25 30 Gly Ser Ser Gly Lys Ala Arg Leu Gln Asp Ala Val Ala Ser Gln Phe 35 40 45 Ala Ala Arg Thr Thr Cys Leu Pro Ser Leu Val Ser Leu Asn His Phe 50 55 60 Pro Ser Gln Phe Cys Val Ser Ser Cys Glu Gly Ala Arg Cys Ser Ser 65 70 75 80 Ala Ser Lys Gln Arg Pro Val Met Pro Arg Ala Thr Ala Ala His Ala 85 90 95 Ser Asn Thr Gln Ser Met Thr Arg Ile Ala Asp Thr Phe Ser Thr Leu 100 105 110 Lys Gln Leu Gly Lys Val Ala Phe Ile Pro Tyr Leu Thr Ala Gly Asp 115 120 125 Pro Asp Leu Asp Thr Thr Ala Gln Ala Leu Arg Leu Leu Asp Asp Cys 130 135 140 Gly Ala Asp Ile Ile Glu Leu Gly Val Pro Tyr Ser Asp Pro Leu Ala 145 150 155 160 Asp Gly Pro Val Ile Gln Ala Ala Ala 165 15 643 DNA Physcomitrella patens CDS (2)..(643) 76_mm2_e11rev 15 g cta cat cat ttt cct act ttt aaa ttt tgt ctt ggt tac cat ttt gga 49 Leu His His Phe Pro Thr Phe Lys Phe Cys Leu Gly Tyr His Phe Gly 1 5 10 15 att gga tcg cga gac gcg cat ttt tct gca ata gct atg gcg ctt gtt 97 Ile Gly Ser Arg Asp Ala His Phe Ser Ala Ile Ala Met Ala Leu Val 20 25 30 agg gga cct atc gga gta gca acc gtc ggc tcg tct ggg aaa gcg cgg 145 Arg Gly Pro Ile Gly Val Ala Thr Val Gly Ser Ser Gly Lys Ala Arg 35 40 45 ctg cag gat gca gtg gcg tct caa ttc gcc gcg cgt acc acg tgc tta 193 Leu Gln Asp Ala Val Ala Ser Gln Phe Ala Ala Arg Thr Thr Cys Leu 50 55 60 cca tcc ctg gtg tcg ctg aac cac ttt cct tcg caa ttc tgc gtt tcc 241 Pro Ser Leu Val Ser Leu Asn His Phe Pro Ser Gln Phe Cys Val Ser 65 70 75 80 tcc tgt gag ggt gct cgt tgt tca agt gca tct aag cag cga cct gtg 289 Ser Cys Glu Gly Ala Arg Cys Ser Ser Ala Ser Lys Gln Arg Pro Val 85 90 95 atg ccc cga gct act gcc gct cac gcc tca aac act cag agc atg act 337 Met Pro Arg Ala Thr Ala Ala His Ala Ser Asn Thr Gln Ser Met Thr 100 105 110 aga att gct gac aca ttt tct aca ctt aag cag cta gga aag gtg gcc 385 Arg Ile Ala Asp Thr Phe Ser Thr Leu Lys Gln Leu Gly Lys Val Ala 115 120 125 ttc att cca tac tta act gcc ggc gac cct gac ttg gat aca acg gct 433 Phe Ile Pro Tyr Leu Thr Ala Gly Asp Pro Asp Leu Asp Thr Thr Ala 130 135 140 cag gca tta cgt cta ctg gat gac tgt gga gca gac atc ata gag ctt 481 Gln Ala Leu Arg Leu Leu Asp Asp Cys Gly Ala Asp Ile Ile Glu Leu 145 150 155 160 gga gtt ccc tac tca gat cct ctt gct gat ggc cct gtc att cag gct 529 Gly Val Pro Tyr Ser Asp Pro Leu Ala Asp Gly Pro Val Ile Gln Ala 165 170 175 gcc gca act agg tcg ctt tcg aag ggc aca act ctc gat aag gtt ttg 577 Ala Ala Thr Arg Ser Leu Ser Lys Gly Thr Thr Leu Asp Lys Val Leu 180 185 190 tcg atg ttg aag gag atc tca cca agc ttg aaa ctc cag ttg tgc ttt 625 Ser Met Leu Lys Glu Ile Ser Pro Ser Leu Lys Leu Gln Leu Cys Phe 195 200 205 tca cat act aca atc cta 643 Ser His Thr Thr Ile Leu 210 16 214 PRT Physcomitrella patens 16 Leu His His Phe Pro Thr Phe Lys Phe Cys Leu Gly Tyr His Phe Gly 1 5 10 15 Ile Gly Ser Arg Asp Ala His Phe Ser Ala Ile Ala Met Ala Leu Val 20 25 30 Arg Gly Pro Ile Gly Val Ala Thr Val Gly Ser Ser Gly Lys Ala Arg 35 40 45 Leu Gln Asp Ala Val Ala Ser Gln Phe Ala Ala Arg Thr Thr Cys Leu 50 55 60 Pro Ser Leu Val Ser Leu Asn His Phe Pro Ser Gln Phe Cys Val Ser 65 70 75 80 Ser Cys Glu Gly Ala Arg Cys Ser Ser Ala Ser Lys Gln Arg Pro Val 85 90 95 Met Pro Arg Ala Thr Ala Ala His Ala Ser Asn Thr Gln Ser Met Thr 100 105 110 Arg Ile Ala Asp Thr Phe Ser Thr Leu Lys Gln Leu Gly Lys Val Ala 115 120 125 Phe Ile Pro Tyr Leu Thr Ala Gly Asp Pro Asp Leu Asp Thr Thr Ala 130 135 140 Gln Ala Leu Arg Leu Leu Asp Asp Cys Gly Ala Asp Ile Ile Glu Leu 145 150 155 160 Gly Val Pro Tyr Ser Asp Pro Leu Ala Asp Gly Pro Val Ile Gln Ala 165 170 175 Ala Ala Thr Arg Ser Leu Ser Lys Gly Thr Thr Leu Asp Lys Val Leu 180 185 190 Ser Met Leu Lys Glu Ile Ser Pro Ser Leu Lys Leu Gln Leu Cys Phe 195 200 205 Ser His Thr Thr Ile Leu 210 17 405 DNA Physcomitrella patens CDS (2)..(403) 94_ppprot3_001_h11 17 c agg att agc agc ctt aaa ctc cat tgc caa gtg agc cca agc tca acc 49 Arg Ile Ser Ser Leu Lys Leu His Cys Gln Val Ser Pro Ser Ser Thr 1 5 10 15 aca ttg cct caa ctc aat gtc gac atc tct ggt cct ggc aag cca ttg 97 Thr Leu Pro Gln Leu Asn Val Asp Ile Ser Gly Pro Gly Lys Pro Leu 20 25 30 cag cct gtg gag cga aca act att cgc ttg gct ctt ccc agc aaa gga 145 Gln Pro Val Glu Arg Thr Thr Ile Arg Leu Ala Leu Pro Ser Lys Gly 35 40 45 cgt atg gcg gaa gac acg ctc ggt ctg atg aag gat tgc cag ctt tca 193 Arg Met Ala Glu Asp Thr Leu Gly Leu Met Lys Asp Cys Gln Leu Ser 50 55 60 gtg cgt aaa ctg aac cct cgc cag tac ata gca gac att tct gaa ctc 241 Val Arg Lys Leu Asn Pro Arg Gln Tyr Ile Ala Asp Ile Ser Glu Leu 65 70 75 80 aag aat gtt gaa gtg tgg ttt caa cga gca tcc gac gtt gtg cgt aag 289 Lys Asn Val Glu Val Trp Phe Gln Arg Ala Ser Asp Val Val Arg Lys 85 90 95 tta aaa act ggg gat gtg gat atg gga att gtt ggc tat gac atg ctt 337 Leu Lys Thr Gly Asp Val Asp Met Gly Ile Val Gly Tyr Asp Met Leu 100 105 110 cgg gag tac ggc gag gat tcc gag gac ctc gta att gtt cac gac gca 385 Arg Glu Tyr Gly Glu Asp Ser Glu Asp Leu Val Ile Val His Asp Ala 115 120 125 ttg gga ttt gga gaa tgt ca 405 Leu Gly Phe Gly Glu Cys 130 18 134 PRT Physcomitrella patens 18 Arg Ile Ser Ser Leu Lys Leu His Cys Gln Val Ser Pro Ser Ser Thr 1 5 10 15 Thr Leu Pro Gln Leu Asn Val Asp Ile Ser Gly Pro Gly Lys Pro Leu 20 25 30 Gln Pro Val Glu Arg Thr Thr Ile Arg Leu Ala Leu Pro Ser Lys Gly 35 40 45 Arg Met Ala Glu Asp Thr Leu Gly Leu Met Lys Asp Cys Gln Leu Ser 50 55 60 Val Arg Lys Leu Asn Pro Arg Gln Tyr Ile Ala Asp Ile Ser Glu Leu 65 70 75 80 Lys Asn Val Glu Val Trp Phe Gln Arg Ala Ser Asp Val Val Arg Lys 85 90 95 Leu Lys Thr Gly Asp Val Asp Met Gly Ile Val Gly Tyr Asp Met Leu 100 105 110 Arg Glu Tyr Gly Glu Asp Ser Glu Asp Leu Val Ile Val His Asp Ala 115 120 125 Leu Gly Phe Gly Glu Cys 130 19 442 DNA Physcomitrella patens CDS (185)..(403) 11_ppprot1_096_b03 19 tttttttttt tttgtgattg gcattttcca actcaaacta aattccatat ttcatacaca 60 gaagagaacc tagaaacgct ctaaaaaatt ctggcctacg tcttacatca agaccacttc 120 ccaaaaatgc tcgggagtga tagacacact ccggattcac atctaccact acaagacaac 180 gtga acc gcc gag gca gaa cct atc atg tgc gtg gag att cat ctc aaa 229 Thr Ala Glu Ala Glu Pro Ile Met Cys Val Glu Ile His Leu Lys 1 5 10 15 gca gat cta tca aaa ccg atc cag aag caa gaa gtc gtt gtc ttc cat 277 Ala Asp Leu Ser Lys Pro Ile Gln Lys Gln Glu Val Val Val Phe His 20 25 30 aac ctg cac atc ttt gtc acc gac aaa atg gtg ccg gcc aat ttg gtt 325 Asn Leu His Ile Phe Val Thr Asp Lys Met Val Pro Ala Asn Leu Val 35 40 45 gac cat ctg aac aaa ttc acg gcg ctt ctc ttt acc cag ggg aac gta 373 Asp His Leu Asn Lys Phe Thr Ala Leu Leu Phe Thr Gln Gly Asn Val 50 55 60 ggg gag acg aaa tac agg tcg aat caa gcc tagctgacat agagctgtat 423 Gly Glu Thr Lys Tyr Arg Ser Asn Gln Ala 65 70 tcaatcctat tgggttggg 442 20 73 PRT Physcomitrella patens 20 Thr Ala Glu Ala Glu Pro Ile Met Cys Val Glu Ile His Leu Lys Ala 1 5 10 15 Asp Leu Ser Lys Pro Ile Gln Lys Gln Glu Val Val Val Phe His Asn 20 25 30 Leu His Ile Phe Val Thr Asp Lys Met Val Pro Ala Asn Leu Val Asp 35 40 45 His Leu Asn Lys Phe Thr Ala Leu Leu Phe Thr Gln Gly Asn Val Gly 50 55 60 Glu Thr Lys Tyr Arg Ser Asn Gln Ala 65 70 21 616 DNA Physcomitrella patens CDS (1)..(615) 34_ppprot3_002_f08 21 cct gag ggg aag act ttg ttt gcc gga gtg gtg gac gga agg aac atc 48 Pro Glu Gly Lys Thr Leu Phe Ala Gly Val Val Asp Gly Arg Asn Ile 1 5 10 15 tgg gcc aac gac ttg gct gcc tct gtg gcc gtg gtt gag gaa ttg cag 96 Trp Ala Asn Asp Leu Ala Ala Ser Val Ala Val Val Glu Glu Leu Gln 20 25 30 gct aag ctt ggg aag gat aac gta gtt gtc tca acc tca tgc tcc ttg 144 Ala Lys Leu Gly Lys Asp Asn Val Val Val Ser Thr Ser Cys Ser Leu 35 40 45 ctc cat tcc gca gtg gac ctc aag aac gag aca aag ttg gat agc gaa 192 Leu His Ser Ala Val Asp Leu Lys Asn Glu Thr Lys Leu Asp Ser Glu 50 55 60 ttg aag tcc tgg atg gca ttc gcc gca cag aag ctg ctg gag gta gtg 240 Leu Lys Ser Trp Met Ala Phe Ala Ala Gln Lys Leu Leu Glu Val Val 65 70 75 80 gcg gtc gct aag gcc gtg tcg gga cag aaa gac gag gct ttc ttc gcg 288 Ala Val Ala Lys Ala Val Ser Gly Gln Lys Asp Glu Ala Phe Phe Ala 85 90 95 gct aac gct tcc gct cag gaa tcg agg agg aac tcc ccc cgc gtt cat 336 Ala Asn Ala Ser Ala Gln Glu Ser Arg Arg Asn Ser Pro Arg Val His 100 105 110 aac aag gca gtg aag gaa gca gcc gct gct ttg gcc ggt tcg gag cac 384 Asn Lys Ala Val Lys Glu Ala Ala Ala Ala Leu Ala Gly Ser Glu His 115 120 125 cgt cga tct acc ccg gta tca agc cgt ctg gaa cag cag cag aag tac 432 Arg Arg Ser Thr Pro Val Ser Ser Arg Leu Glu Gln Gln Gln Lys Tyr 130 135 140 ttg aac ctg cca atc ctg ccg acg acc acg atc gga tcg ttc ccc cag 480 Leu Asn Leu Pro Ile Leu Pro Thr Thr Thr Ile Gly Ser Phe Pro Gln 145 150 155 160 acg cca gag ctc cgc agg gtc agg cgt gag gtg aag agc aag aag atc 528 Thr Pro Glu Leu Arg Arg Val Arg Arg Glu Val Lys Ser Lys Lys Ile 165 170 175 tca gag gag gat tat gac aag gcc atc aag gca gag att gac agt gtg 576 Ser Glu Glu Asp Tyr Asp Lys Ala Ile Lys Ala Glu Ile Asp Ser Val 180 185 190 gtg aag ctg caa gag gag ctg gac att gat gtg ctg gtc c 616 Val Lys Leu Gln Glu Glu Leu Asp Ile Asp Val Leu Val 195 200 205 22 205 PRT Physcomitrella patens 22 Pro Glu Gly Lys Thr Leu Phe Ala Gly Val Val Asp Gly Arg Asn Ile 1 5 10 15 Trp Ala Asn Asp Leu Ala Ala Ser Val Ala Val Val Glu Glu Leu Gln 20 25 30 Ala Lys Leu Gly Lys Asp Asn Val Val Val Ser Thr Ser Cys Ser Leu 35 40 45 Leu His Ser Ala Val Asp Leu Lys Asn Glu Thr Lys Leu Asp Ser Glu 50 55 60 Leu Lys Ser Trp Met Ala Phe Ala Ala Gln Lys Leu Leu Glu Val Val 65 70 75 80 Ala Val Ala Lys Ala Val Ser Gly Gln Lys Asp Glu Ala Phe Phe Ala 85 90 95 Ala Asn Ala Ser Ala Gln Glu Ser Arg Arg Asn Ser Pro Arg Val His 100 105 110 Asn Lys Ala Val Lys Glu Ala Ala Ala Ala Leu Ala Gly Ser Glu His 115 120 125 Arg Arg Ser Thr Pro Val Ser Ser Arg Leu Glu Gln Gln Gln Lys Tyr 130 135 140 Leu Asn Leu Pro Ile Leu Pro Thr Thr Thr Ile Gly Ser Phe Pro Gln 145 150 155 160 Thr Pro Glu Leu Arg Arg Val Arg Arg Glu Val Lys Ser Lys Lys Ile 165 170 175 Ser Glu Glu Asp Tyr Asp Lys Ala Ile Lys Ala Glu Ile Asp Ser Val 180 185 190 Val Lys Leu Gln Glu Glu Leu Asp Ile Asp Val Leu Val 195 200 205 23 609 DNA Physcomitrella patens CDS (3)..(608) 94_ppprot1_072_h11 23 ct gca ctc gac atg gcg gct ctt cgg caa gtg agt aat gcg aca ctg 47 Ala Leu Asp Met Ala Ala Leu Arg Gln Val Ser Asn Ala Thr Leu 1 5 10 15 ggt tgt gct gct gca ccc caa gtt gtg aag gcg ggt gac tca acg gtg 95 Gly Cys Ala Ala Ala Pro Gln Val Val Lys Ala Gly Asp Ser Thr Val 20 25 30 aga agg gtg aac atg gcg tct ttg gag tca gcg atg gcg ggt ctg cag 143 Arg Arg Val Asn Met Ala Ser Leu Glu Ser Ala Met Ala Gly Leu Gln 35 40 45 ttg aag gga atg agg acc gga ccc aac gtg gtg gag aga gcc aag agg 191 Leu Lys Gly Met Arg Thr Gly Pro Asn Val Val Glu Arg Ala Lys Arg 50 55 60 acg agt gtg gtc agc cag gcc gtc tcc acc gag aag gag ctg gag ttg 239 Thr Ser Val Val Ser Gln Ala Val Ser Thr Glu Lys Glu Leu Glu Leu 65 70 75 aac atc gcc gat gat gtt acc cag ttg att ggt aaa acg cct atg gta 287 Asn Ile Ala Asp Asp Val Thr Gln Leu Ile Gly Lys Thr Pro Met Val 80 85 90 95 tac ctc aat aca gtg gtg gaa gga tgc acc gcc aat att gcg gcc aag 335 Tyr Leu Asn Thr Val Val Glu Gly Cys Thr Ala Asn Ile Ala Ala Lys 100 105 110 ttg gag ata atg gag ccc tgt tgc agt gtt aag gat agg att ggt ttt 383 Leu Glu Ile Met Glu Pro Cys Cys Ser Val Lys Asp Arg Ile Gly Phe 115 120 125 agc atg att act gat gcg gag aat aag ggt gca att act ccc gga aag 431 Ser Met Ile Thr Asp Ala Glu Asn Lys Gly Ala Ile Thr Pro Gly Lys 130 135 140 agc att ctt gtt gag cca acc agt ggg aac acc ggt att ggt ttg gct 479 Ser Ile Leu Val Glu Pro Thr Ser Gly Asn Thr Gly Ile Gly Leu Ala 145 150 155 ttc att gcg gct gcc aaa ggt tac aag ctt atc ctt acc atg cct gca 527 Phe Ile Ala Ala Ala Lys Gly Tyr Lys Leu Ile Leu Thr Met Pro Ala 160 165 170 175 tcc atg agt ttg gag cgg cgc att ctg ttg aaa gct ttt gga gcg gag 575 Ser Met Ser Leu Glu Arg Arg Ile Leu Leu Lys Ala Phe Gly Ala Glu 180 185 190 ctt gtc ctt acc gac cca gct aag gga atg aaa g 609 Leu Val Leu Thr Asp Pro Ala Lys Gly Met Lys 195 200 24 202 PRT Physcomitrella patens 24 Ala Leu Asp Met Ala Ala Leu Arg Gln Val Ser Asn Ala Thr Leu Gly 1 5 10 15 Cys Ala Ala Ala Pro Gln Val Val Lys Ala Gly Asp Ser Thr Val Arg 20 25 30 Arg Val Asn Met Ala Ser Leu Glu Ser Ala Met Ala Gly Leu Gln Leu 35 40 45 Lys Gly Met Arg Thr Gly Pro Asn Val Val Glu Arg Ala Lys Arg Thr 50 55 60 Ser Val Val Ser Gln Ala Val Ser Thr Glu Lys Glu Leu Glu Leu Asn 65 70 75 80 Ile Ala Asp Asp Val Thr Gln Leu Ile Gly Lys Thr Pro Met Val Tyr 85 90 95 Leu Asn Thr Val Val Glu Gly Cys Thr Ala Asn Ile Ala Ala Lys Leu 100 105 110 Glu Ile Met Glu Pro Cys Cys Ser Val Lys Asp Arg Ile Gly Phe Ser 115 120 125 Met Ile Thr Asp Ala Glu Asn Lys Gly Ala Ile Thr Pro Gly Lys Ser 130 135 140 Ile Leu Val Glu Pro Thr Ser Gly Asn Thr Gly Ile Gly Leu Ala Phe 145 150 155 160 Ile Ala Ala Ala Lys Gly Tyr Lys Leu Ile Leu Thr Met Pro Ala Ser 165 170 175 Met Ser Leu Glu Arg Arg Ile Leu Leu Lys Ala Phe Gly Ala Glu Leu 180 185 190 Val Leu Thr Asp Pro Ala Lys Gly Met Lys 195 200 25 385 DNA Physcomitrella patens CDS (2)..(355) 02_ck18_a07fwd 25 c cga gtt act ggc aac ttg gaa ggc tgg gga ctt cca gag aga gat ggg 49 Arg Val Thr Gly Asn Leu Glu Gly Trp Gly Leu Pro Glu Arg Asp Gly 1 5 10 15 ggt tgc att gat ttc tgg tgc cag gtt act gat gaa gag gct ttg cca 97 Gly Cys Ile Asp Phe Trp Cys Gln Val Thr Asp Glu Glu Ala Leu Pro 20 25 30 ctc atc tac gat ctg ctc aag caa gaa ggc ttc tgc atg ggc ggt tca 145 Leu Ile Tyr Asp Leu Leu Lys Gln Glu Gly Phe Cys Met Gly Gly Ser 35 40 45 aca gcc atc aat att ggt ggg gca atc aaa ctg gcc aag cag ctg ggt 193 Thr Ala Ile Asn Ile Gly Gly Ala Ile Lys Leu Ala Lys Gln Leu Gly 50 55 60 ccc ggt cac act att gtg acc att ctt tgc gat ctt gga acg agg tac 241 Pro Gly His Thr Ile Val Thr Ile Leu Cys Asp Leu Gly Thr Arg Tyr 65 70 75 80 caa agt aag ata ttc aac gtt gat ttt ctc aag tca aaa gga cta cca 289 Gln Ser Lys Ile Phe Asn Val Asp Phe Leu Lys Ser Lys Gly Leu Pro 85 90 95 ttt cca gaa tgg ttg gac ccc gct aat caa gac acc agc ata ccc gag 337 Phe Pro Glu Trp Leu Asp Pro Ala Asn Gln Asp Thr Ser Ile Pro Glu 100 105 110 gtt ttc gag cag gtc gag tgatgtcctc agattgaacc cttttcactg 385 Val Phe Glu Gln Val Glu 115 26 118 PRT Physcomitrella patens 26 Arg Val Thr Gly Asn Leu Glu Gly Trp Gly Leu Pro Glu Arg Asp Gly 1 5 10 15 Gly Cys Ile Asp Phe Trp Cys Gln Val Thr Asp Glu Glu Ala Leu Pro 20 25 30 Leu Ile Tyr Asp Leu Leu Lys Gln Glu Gly Phe Cys Met Gly Gly Ser 35 40 45 Thr Ala Ile Asn Ile Gly Gly Ala Ile Lys Leu Ala Lys Gln Leu Gly 50 55 60 Pro Gly His Thr Ile Val Thr Ile Leu Cys Asp Leu Gly Thr Arg Tyr 65 70 75 80 Gln Ser Lys Ile Phe Asn Val Asp Phe Leu Lys Ser Lys Gly Leu Pro 85 90 95 Phe Pro Glu Trp Leu Asp Pro Ala Asn Gln Asp Thr Ser Ile Pro Glu 100 105 110 Val Phe Glu Gln Val Glu 115 27 568 DNA Physcomitrella patens CDS (1)..(492) 72_ck11_d12fwd 27 gtc gcc aac att gcg gcc aag ttg gag atc atg gag cct tgc tgc agt 48 Val Ala Asn Ile Ala Ala Lys Leu Glu Ile Met Glu Pro Cys Cys Ser 1 5 10 15 gtc aag gat agg att gga ttc agc atg atc act gac gca gag agc aag 96 Val Lys Asp Arg Ile Gly Phe Ser Met Ile Thr Asp Ala Glu Ser Lys 20 25 30 ggt gcg att act cca gga aag agc atc ctt gtg gag ccg acc agt ggc 144 Gly Ala Ile Thr Pro Gly Lys Ser Ile Leu Val Glu Pro Thr Ser Gly 35 40 45 aac acc ggc att ggc ttg gct ttc atc gct gct gcc aaa ggg tac aag 192 Asn Thr Gly Ile Gly Leu Ala Phe Ile Ala Ala Ala Lys Gly Tyr Lys 50 55 60 ctc atc ctc act atg cct gca tca atg agt ttg gag cga cgt att cta 240 Leu Ile Leu Thr Met Pro Ala Ser Met Ser Leu Glu Arg Arg Ile Leu 65 70 75 80 ttg agg gcc ttc ggc gcg gaa ctc att ctt acc gac cca gcc aag gga 288 Leu Arg Ala Phe Gly Ala Glu Leu Ile Leu Thr Asp Pro Ala Lys Gly 85 90 95 atg aaa ggc gct gtt cag aag gcg gaa gaa att gtg aag aaa act ccc 336 Met Lys Gly Ala Val Gln Lys Ala Glu Glu Ile Val Lys Lys Thr Pro 100 105 110 aat tcg tac atg ctc caa caa ttt gag aat cca gct aac ccg aag gtg 384 Asn Ser Tyr Met Leu Gln Gln Phe Glu Asn Pro Ala Asn Pro Lys Val 115 120 125 cat ttt gag acc acc ggg cca gag atc tgg gaa gac acg gct ggt aag 432 His Phe Glu Thr Thr Gly Pro Glu Ile Trp Glu Asp Thr Ala Gly Lys 130 135 140 gtt gat att ctc gtt gct ggt att ggt act ggc gga act gta act gga 480 Val Asp Ile Leu Val Ala Gly Ile Gly Thr Gly Gly Thr Val Thr Gly 145 150 155 160 gcc ggt cgc ttt tgaaaagcca aaaccctggt gtgaaagtta ttggagttga 532 Ala Gly Arg Phe gccaactgag acagtgtact ttctggaggc aagcca 568 28 164 PRT Physcomitrella patens 28 Val Ala Asn Ile Ala Ala Lys Leu Glu Ile Met Glu Pro Cys Cys Ser 1 5 10 15 Val Lys Asp Arg Ile Gly Phe Ser Met Ile Thr Asp Ala Glu Ser Lys 20 25 30 Gly Ala Ile Thr Pro Gly Lys Ser Ile Leu Val Glu Pro Thr Ser Gly 35 40 45 Asn Thr Gly Ile Gly Leu Ala Phe Ile Ala Ala Ala Lys Gly Tyr Lys 50 55 60 Leu Ile Leu Thr Met Pro Ala Ser Met Ser Leu Glu Arg Arg Ile Leu 65 70 75 80 Leu Arg Ala Phe Gly Ala Glu Leu Ile Leu Thr Asp Pro Ala Lys Gly 85 90 95 Met Lys Gly Ala Val Gln Lys Ala Glu Glu Ile Val Lys Lys Thr Pro 100 105 110 Asn Ser Tyr Met Leu Gln Gln Phe Glu Asn Pro Ala Asn Pro Lys Val 115 120 125 His Phe Glu Thr Thr Gly Pro Glu Ile Trp Glu Asp Thr Ala Gly Lys 130 135 140 Val Asp Ile Leu Val Ala Gly Ile Gly Thr Gly Gly Thr Val Thr Gly 145 150 155 160 Ala Gly Arg Phe 29 519 DNA Physcomitrella patens CDS (1)..(519) 41_ppprot1_054_g03 29 gtt ttc aag tac agc cag aaa agg cct gat tgc tgc agc tgc aat ctt 48 Val Phe Lys Tyr Ser Gln Lys Arg Pro Asp Cys Cys Ser Cys Asn Leu 1 5 10 15 gga aat tca ggc ctc gat agt gca tgc aca ttg caa aaa cag ctg atc 96 Gly Asn Ser Gly Leu Asp Ser Ala Cys Thr Leu Gln Lys Gln Leu Ile 20 25 30 acg ctt aac gcg atg gga gtc tcc gta gcc tca ccg gtt ttg agc aat 144 Thr Leu Asn Ala Met Gly Val Ser Val Ala Ser Pro Val Leu Ser Asn 35 40 45 gag gtt ctt gga cat cac gac gcg gat ctg ctg aag acg aag cta gtt 192 Glu Val Leu Gly His His Asp Ala Asp Leu Leu Lys Thr Lys Leu Val 50 55 60 tcc aac ggc ggc ttc caa ccc ccc aag ctg ctg cag gaa gaa atg gca 240 Ser Asn Gly Gly Phe Gln Pro Pro Lys Leu Leu Gln Glu Glu Met Ala 65 70 75 80 ccg tct tcg atc ata aag agc ctg acc gtt gtg gac acg gac gaa ttc 288 Pro Ser Ser Ile Ile Lys Ser Leu Thr Val Val Asp Thr Asp Glu Phe 85 90 95 gac gac gat tcg aca tcc gag gac gag aag gtg atg gaa tat gtg aag 336 Asp Asp Asp Ser Thr Ser Glu Asp Glu Lys Val Met Glu Tyr Val Lys 100 105 110 gaa atc ccg att acc gac gtc gat gag cga gac aag ggc acc tcg gac 384 Glu Ile Pro Ile Thr Asp Val Asp Glu Arg Asp Lys Gly Thr Ser Asp 115 120 125 gac tgg att ccg cgc cac ccc gag ctg gtc cgc ctc acc ggc cga cac 432 Asp Trp Ile Pro Arg His Pro Glu Leu Val Arg Leu Thr Gly Arg His 130 135 140 ccc ttc aac tgc gag cca ccg ctg tcc acc ttg atg gag gcc gga ttc 480 Pro Phe Asn Cys Glu Pro Pro Leu Ser Thr Leu Met Glu Ala Gly Phe 145 150 155 160 ctg acg ccg acg tcc ctg cac tac gtt cga aac cac ggg 519 Leu Thr Pro Thr Ser Leu His Tyr Val Arg Asn His Gly 165 170 30 173 PRT Physcomitrella patens 30 Val Phe Lys Tyr Ser Gln Lys Arg Pro Asp Cys Cys Ser Cys Asn Leu 1 5 10 15 Gly Asn Ser Gly Leu Asp Ser Ala Cys Thr Leu Gln Lys Gln Leu Ile 20 25 30 Thr Leu Asn Ala Met Gly Val Ser Val Ala Ser Pro Val Leu Ser Asn 35 40 45 Glu Val Leu Gly His His Asp Ala Asp Leu Leu Lys Thr Lys Leu Val 50 55 60 Ser Asn Gly Gly Phe Gln Pro Pro Lys Leu Leu Gln Glu Glu Met Ala 65 70 75 80 Pro Ser Ser Ile Ile Lys Ser Leu Thr Val Val Asp Thr Asp Glu Phe 85 90 95 Asp Asp Asp Ser Thr Ser Glu Asp Glu Lys Val Met Glu Tyr Val Lys 100 105 110 Glu Ile Pro Ile Thr Asp Val Asp Glu Arg Asp Lys Gly Thr Ser Asp 115 120 125 Asp Trp Ile Pro Arg His Pro Glu Leu Val Arg Leu Thr Gly Arg His 130 135 140 Pro Phe Asn Cys Glu Pro Pro Leu Ser Thr Leu Met Glu Ala Gly Phe 145 150 155 160 Leu Thr Pro Thr Ser Leu His Tyr Val Arg Asn His Gly 165 170 31 554 DNA Physcomitrella patens CDS (2)..(553) 54_ppprot3_002_a12 31 c aac aaa gtg tac gat tgc acg ccg ttt ctg aac gac cat ccg ggc ggc 49 Asn Lys Val Tyr Asp Cys Thr Pro Phe Leu Asn Asp His Pro Gly Gly 1 5 10 15 gcg gac agc atc ctg atc aac gga ggc atg gat tcg acg gag gag ttc 97 Ala Asp Ser Ile Leu Ile Asn Gly Gly Met Asp Ser Thr Glu Glu Phe 20 25 30 gac gcc att cac tcc gcc aaa gcc cag acc atg ttg gag gag tac tac 145 Asp Ala Ile His Ser Ala Lys Ala Gln Thr Met Leu Glu Glu Tyr Tyr 35 40 45 att gga gac ctg tcg gcg tcg acg gct gag gtg gtg gat gtg gcg ccc 193 Ile Gly Asp Leu Ser Ala Ser Thr Ala Glu Val Val Asp Val Ala Pro 50 55 60 aag aca gaa gcg gag gcg att cca aca gcg ttg tct gca tca gga agg 241 Lys Thr Glu Ala Glu Ala Ile Pro Thr Ala Leu Ser Ala Ser Gly Arg 65 70 75 80 ccg gtt gct ctg agc ctc aag gaa cgg atc gcc ttc cgc ctg atc gag 289 Pro Val Ala Leu Ser Leu Lys Glu Arg Ile Ala Phe Arg Leu Ile Glu 85 90 95 agg gag gtt ctg agt cac gac gtt cgg agg ctg aga ttc gca ctc cag 337 Arg Glu Val Leu Ser His Asp Val Arg Arg Leu Arg Phe Ala Leu Gln 100 105 110 agc gag aat cac gtg ctg gga ctg ccg gtg ggc aag cac gtc ctc ctg 385 Ser Glu Asn His Val Leu Gly Leu Pro Val Gly Lys His Val Leu Leu 115 120 125 agc gca tcc atc aac ggg aag ctg tgc atg agg gct tac act ccc acc 433 Ser Ala Ser Ile Asn Gly Lys Leu Cys Met Arg Ala Tyr Thr Pro Thr 130 135 140 agc aac gac gac gat gtg ggg tac ctg gag ctg gtg ata aag gtg tac 481 Ser Asn Asp Asp Asp Val Gly Tyr Leu Glu Leu Val Ile Lys Val Tyr 145 150 155 160 ttc aag gac gtg cac ccc aag ttt ccg atg gga ggc atg ttc tct cag 529 Phe Lys Asp Val His Pro Lys Phe Pro Met Gly Gly Met Phe Ser Gln 165 170 175 cac ctg gac acg ctg aga gtc ggc g 554 His Leu Asp Thr Leu Arg Val Gly 180 32 184 PRT Physcomitrella patens 32 Asn Lys Val Tyr Asp Cys Thr Pro Phe Leu Asn Asp His Pro Gly Gly 1 5 10 15 Ala Asp Ser Ile Leu Ile Asn Gly Gly Met Asp Ser Thr Glu Glu Phe 20 25 30 Asp Ala Ile His Ser Ala Lys Ala Gln Thr Met Leu Glu Glu Tyr Tyr 35 40 45 Ile Gly Asp Leu Ser Ala Ser Thr Ala Glu Val Val Asp Val Ala Pro 50 55 60 Lys Thr Glu Ala Glu Ala Ile Pro Thr Ala Leu Ser Ala Ser Gly Arg 65 70 75 80 Pro Val Ala Leu Ser Leu Lys Glu Arg Ile Ala Phe Arg Leu Ile Glu 85 90 95 Arg Glu Val Leu Ser His Asp Val Arg Arg Leu Arg Phe Ala Leu Gln 100 105 110 Ser Glu Asn His Val Leu Gly Leu Pro Val Gly Lys His Val Leu Leu 115 120 125 Ser Ala Ser Ile Asn Gly Lys Leu Cys Met Arg Ala Tyr Thr Pro Thr 130 135 140 Ser Asn Asp Asp Asp Val Gly Tyr Leu Glu Leu Val Ile Lys Val Tyr 145 150 155 160 Phe Lys Asp Val His Pro Lys Phe Pro Met Gly Gly Met Phe Ser Gln 165 170 175 His Leu Asp Thr Leu Arg Val Gly 180 33 531 DNA Physcomitrella patens CDS (114)..(530) 71_ppprot1_60_d06 33 gggtcagcct agaaacccat ttctctggta cattactgaa ctacactgta agtgttgatt 60 cattgcaatc tggtatcctc tgctgtttcc gtgaagagtg gagcattgtc tga gtg 116 Val 1 aag gaa ctg aaa ttt gaa gcc atg gag tca acg ctg acg aga gct tgg 164 Lys Glu Leu Lys Phe Glu Ala Met Glu Ser Thr Leu Thr Arg Ala Trp 5 10 15 gct gct acc agc ttt agt gcg ctg aaa acc gca tca gtg agt gcg tcc 212 Ala Ala Thr Ser Phe Ser Ala Leu Lys Thr Ala Ser Val Ser Ala Ser 20 25 30 ccg cga atg ctg agt tcc acc gca ttt ttt ctt gga act tca gtg aag 260 Pro Arg Met Leu Ser Ser Thr Ala Phe Phe Leu Gly Thr Ser Val Lys 35 40 45 ctt aat gga ggg ttg tct tcg tgg cag gcg gga tct caa tgt cga ggt 308 Leu Asn Gly Gly Leu Ser Ser Trp Gln Ala Gly Ser Gln Cys Arg Gly 50 55 60 65 atc ccc tgt ccc aag aga ctc aat cag agg ctg cag gta tca gca gca 356 Ile Pro Cys Pro Lys Arg Leu Asn Gln Arg Leu Gln Val Ser Ala Ala 70 75 80 atc aaa gaa gtg acg gga tcc tta atg aag ggc gag ggt cta aaa ttt 404 Ile Lys Glu Val Thr Gly Ser Leu Met Lys Gly Glu Gly Leu Lys Phe 85 90 95 ggc gtg gtt gtg ggt cgc ttc aat gaa gtc ata act agg cct cta ctt 452 Gly Val Val Val Gly Arg Phe Asn Glu Val Ile Thr Arg Pro Leu Leu 100 105 110 gcg gga gct ctg gat gcg ttc cat aga tat caa gtg cga gaa gag gat 500 Ala Gly Ala Leu Asp Ala Phe His Arg Tyr Gln Val Arg Glu Glu Asp 115 120 125 atc gac gtg atc tgg gtg cct gga agc ttt g 531 Ile Asp Val Ile Trp Val Pro Gly Ser Phe 130 135 34 139 PRT Physcomitrella patens 34 Val Lys Glu Leu Lys Phe Glu Ala Met Glu Ser Thr Leu Thr Arg Ala 1 5 10 15 Trp Ala Ala Thr Ser Phe Ser Ala Leu Lys Thr Ala Ser Val Ser Ala 20 25 30 Ser Pro Arg Met Leu Ser Ser Thr Ala Phe Phe Leu Gly Thr Ser Val 35 40 45 Lys Leu Asn Gly Gly Leu Ser Ser Trp Gln Ala Gly Ser Gln Cys Arg 50 55 60 Gly Ile Pro Cys Pro Lys Arg Leu Asn Gln Arg Leu Gln Val Ser Ala 65 70 75 80 Ala Ile Lys Glu Val Thr Gly Ser Leu Met Lys Gly Glu Gly Leu Lys 85 90 95 Phe Gly Val Val Val Gly Arg Phe Asn Glu Val Ile Thr Arg Pro Leu 100 105 110 Leu Ala Gly Ala Leu Asp Ala Phe His Arg Tyr Gln Val Arg Glu Glu 115 120 125 Asp Ile Asp Val Ile Trp Val Pro Gly Ser Phe 130 135 35 324 DNA Physcomitrella patens CDS (3)..(323) 32_ck1_f07fwd 35 gt gta tcg ttt ctg gga acg cca gtg aag ctt aat gga cgg ctg gct 47 Val Ser Phe Leu Gly Thr Pro Val Lys Leu Asn Gly Arg Leu Ala 1 5 10 15 tcg tat caa ggt gca tct gaa cat gga ggt ttc ctc cac acc agg aga 95 Ser Tyr Gln Gly Ala Ser Glu His Gly Gly Phe Leu His Thr Arg Arg 20 25 30 gtc agt cag agg ctc cag gta tca gca gca gtc aag gag gtg act gga 143 Val Ser Gln Arg Leu Gln Val Ser Ala Ala Val Lys Glu Val Thr Gly 35 40 45 tcc tta gtg aag ggc gca ggt ctt cga ttt ggc gtg gta gtt ggt cgc 191 Ser Leu Val Lys Gly Ala Gly Leu Arg Phe Gly Val Val Val Gly Arg 50 55 60 ttc aat gaa atc ata act aag cct ctg ctg gcg gga gct ctc gat gca 239 Phe Asn Glu Ile Ile Thr Lys Pro Leu Leu Ala Gly Ala Leu Asp Ala 65 70 75 ttc tac aaa cat caa gtg cgg gaa gag gat ata gac gtg aca tgg gtg 287 Phe Tyr Lys His Gln Val Arg Glu Glu Asp Ile Asp Val Thr Trp Val 80 85 90 95 cca gga agc ttt gaa att ccg gtg gtt gct caa cag c 324 Pro Gly Ser Phe Glu Ile Pro Val Val Ala Gln Gln 100 105 36 107 PRT Physcomitrella patens 36 Val Ser Phe Leu Gly Thr Pro Val Lys Leu Asn Gly Arg Leu Ala Ser 1 5 10 15 Tyr Gln Gly Ala Ser Glu His Gly Gly Phe Leu His Thr Arg Arg Val 20 25 30 Ser Gln Arg Leu Gln Val Ser Ala Ala Val Lys Glu Val Thr Gly Ser 35 40 45 Leu Val Lys Gly Ala Gly Leu Arg Phe Gly Val Val Val Gly Arg Phe 50 55 60 Asn Glu Ile Ile Thr Lys Pro Leu Leu Ala Gly Ala Leu Asp Ala Phe 65 70 75 80 Tyr Lys His Gln Val Arg Glu Glu Asp Ile Asp Val Thr Trp Val Pro 85 90 95 Gly Ser Phe Glu Ile Pro Val Val Ala Gln Gln 100 105 37 502 DNA Physcomitrella patens CDS (2)..(502) 78_ck8_e12fwd 37 g aaa tac cct tcg gtg gtc acg gga tac acc act cag tac acg ttt cac 49 Lys Tyr Pro Ser Val Val Thr Gly Tyr Thr Thr Gln Tyr Thr Phe His 1 5 10 15 cac tat aca tct ggt ttc att cac cat gtg gtt att tcc gac ttg gag 97 His Tyr Thr Ser Gly Phe Ile His His Val Val Ile Ser Asp Leu Glu 20 25 30 ttc aac acc aag tat ttc tac aaa gtt ggg gaa gag gag gaa ggt gcc 145 Phe Asn Thr Lys Tyr Phe Tyr Lys Val Gly Glu Glu Glu Glu Gly Ala 35 40 45 cgt gag ttt ttt ttc aca act cct cct gct cct gga cca gac aca ccc 193 Arg Glu Phe Phe Phe Thr Thr Pro Pro Ala Pro Gly Pro Asp Thr Pro 50 55 60 tac gct ttt gga gtt ata ggg gac ttg ggt cag acg ttt gat tca gct 241 Tyr Ala Phe Gly Val Ile Gly Asp Leu Gly Gln Thr Phe Asp Ser Ala 65 70 75 80 acc aca gtg gag cat tac ttg aag agt tac ggc cag aca gtt ctt ttc 289 Thr Thr Val Glu His Tyr Leu Lys Ser Tyr Gly Gln Thr Val Leu Phe 85 90 95 gtc ggc gac cta gct tac cag gac act tac cca ttt cac tat caa gtc 337 Val Gly Asp Leu Ala Tyr Gln Asp Thr Tyr Pro Phe His Tyr Gln Val 100 105 110 cgt ttt gac aca tgg agc cga ttc gtt gaa cgc agt gcg gcc tat cag 385 Arg Phe Asp Thr Trp Ser Arg Phe Val Glu Arg Ser Ala Ala Tyr Gln 115 120 125 cca tgg ata tgg aca aca ggg aac cac gag att gat ttt ctc cct cac 433 Pro Trp Ile Trp Thr Thr Gly Asn His Glu Ile Asp Phe Leu Pro His 130 135 140 atc gga gaa att act cca ttc aaa ccc ttc aat cat cga ttc cct aca 481 Ile Gly Glu Ile Thr Pro Phe Lys Pro Phe Asn His Arg Phe Pro Thr 145 150 155 160 cct cac gac gca tcc agc agc 502 Pro His Asp Ala Ser Ser Ser 165 38 167 PRT Physcomitrella patens 38 Lys Tyr Pro Ser Val Val Thr Gly Tyr Thr Thr Gln Tyr Thr Phe His 1 5 10 15 His Tyr Thr Ser Gly Phe Ile His His Val Val Ile Ser Asp Leu Glu 20 25 30 Phe Asn Thr Lys Tyr Phe Tyr Lys Val Gly Glu Glu Glu Glu Gly Ala 35 40 45 Arg Glu Phe Phe Phe Thr Thr Pro Pro Ala Pro Gly Pro Asp Thr Pro 50 55 60 Tyr Ala Phe Gly Val Ile Gly Asp Leu Gly Gln Thr Phe Asp Ser Ala 65 70 75 80 Thr Thr Val Glu His Tyr Leu Lys Ser Tyr Gly Gln Thr Val Leu Phe 85 90 95 Val Gly Asp Leu Ala Tyr Gln Asp Thr Tyr Pro Phe His Tyr Gln Val 100 105 110 Arg Phe Asp Thr Trp Ser Arg Phe Val Glu Arg Ser Ala Ala Tyr Gln 115 120 125 Pro Trp Ile Trp Thr Thr Gly Asn His Glu Ile Asp Phe Leu Pro His 130 135 140 Ile Gly Glu Ile Thr Pro Phe Lys Pro Phe Asn His Arg Phe Pro Thr 145 150 155 160 Pro His Asp Ala Ser Ser Ser 165 39 532 DNA Physcomitrella patens CDS (1)..(291) 25_ppprot1_098_e01 39 ctc acc tac ccc atc ttc ccg aat gaa gaa cta tct gcc att gcc aaa 48 Leu Thr Tyr Pro Ile Phe Pro Asn Glu Glu Leu Ser Ala Ile Ala Lys 1 5 10 15 aag ttt ggc cat act gag gag gag ctg cag gtt gca aac acg ctg ccg 96 Lys Phe Gly His Thr Glu Glu Glu Leu Gln Val Ala Asn Thr Leu Pro 20 25 30 aac tct acc att gct gcc tac acg acg ttg ctt gtt cca cag ggg acc 144 Asn Ser Thr Ile Ala Ala Tyr Thr Thr Leu Leu Val Pro Gln Gly Thr 35 40 45 tca act ccc ggt ggt aat gct ggg gga cct ggc tca gct cca gct cca 192 Ser Thr Pro Gly Gly Asn Ala Gly Gly Pro Gly Ser Ala Pro Ala Pro 50 55 60 tct gca gct tca aga gct tcc caa gcc cac tgg ctg tac tca gtc tcc 240 Ser Ala Ala Ser Arg Ala Ser Gln Ala His Trp Leu Tyr Ser Val Ser 65 70 75 80 ttg ctg gga gtg caa tct ttg ttg ctg ttg ttg ttg ttc tac cat gct 288 Leu Leu Gly Val Gln Ser Leu Leu Leu Leu Leu Leu Phe Tyr His Ala 85 90 95 aag taagagagag tgcagaggtg agattgtgtg aagtagatag ccctccatca 341 Lys ccatcctacc aattccctcc tcctccatct gtcttctaac cttctctttt tcccctcatt 401 gtgtcctttt gtgtgacctt tcagggttcc tagctaccgc aactctttcc agctttgcat 461 cttttttgtg ctaaaaccag cgctcttgta ggtgttttgt gatcaataga aacatgcgct 521 tagtgtgtgt g 532 40 97 PRT Physcomitrella patens 40 Leu Thr Tyr Pro Ile Phe Pro Asn Glu Glu Leu Ser Ala Ile Ala Lys 1 5 10 15 Lys Phe Gly His Thr Glu Glu Glu Leu Gln Val Ala Asn Thr Leu Pro 20 25 30 Asn Ser Thr Ile Ala Ala Tyr Thr Thr Leu Leu Val Pro Gln Gly Thr 35 40 45 Ser Thr Pro Gly Gly Asn Ala Gly Gly Pro Gly Ser Ala Pro Ala Pro 50 55 60 Ser Ala Ala Ser Arg Ala Ser Gln Ala His Trp Leu Tyr Ser Val Ser 65 70 75 80 Leu Leu Gly Val Gln Ser Leu Leu Leu Leu Leu Leu Phe Tyr His Ala 85 90 95 Lys 41 539 DNA Physcomitrella patens CDS (1)..(537) 35_ppprot1_099_f03 41 gaa gaa cac ttg gac agg ctt ttt gat tca gct aaa gca atg gcc ttt 48 Glu Glu His Leu Asp Arg Leu Phe Asp Ser Ala Lys Ala Met Ala Phe 1 5 10 15 gcc aat gtt cct agt cga agt gag gtg aag cgg gct tta ttt gcc acc 96 Ala Asn Val Pro Ser Arg Ser Glu Val Lys Arg Ala Leu Phe Ala Thr 20 25 30 ctc ata gca aac aac atg cga gat aat gca cat gtc aga cta aca ctt 144 Leu Ile Ala Asn Asn Met Arg Asp Asn Ala His Val Arg Leu Thr Leu 35 40 45 aca cgc gga gag aag act aca tca gga atg agt cca gct ttt aac gtc 192 Thr Arg Gly Glu Lys Thr Thr Ser Gly Met Ser Pro Ala Phe Asn Val 50 55 60 tat gga tgc aat tta att gta cta gct gag tgg aag cca cct gta tat 240 Tyr Gly Cys Asn Leu Ile Val Leu Ala Glu Trp Lys Pro Pro Val Tyr 65 70 75 80 aac aac acg gat ggc ata tgt ctc atc acg gca tca act cgt cgt aac 288 Asn Asn Thr Asp Gly Ile Cys Leu Ile Thr Ala Ser Thr Arg Arg Asn 85 90 95 tct ccc aat agt ttg aat tcc aag atc cac cac aat aat ctc atc aac 336 Ser Pro Asn Ser Leu Asn Ser Lys Ile His His Asn Asn Leu Ile Asn 100 105 110 aac ata tta gcc aag gtt gaa ggc aat cta gct ggt gca gga gac gca 384 Asn Ile Leu Ala Lys Val Glu Gly Asn Leu Ala Gly Ala Gly Asp Ala 115 120 125 tta atg ctt gat tgt gat gga ttt gtt tct gaa acg aat gcc act aat 432 Leu Met Leu Asp Cys Asp Gly Phe Val Ser Glu Thr Asn Ala Thr Asn 130 135 140 atc ttc atg gtg aag aaa gga cgg gtt ttg act cct cat gct gac tat 480 Ile Phe Met Val Lys Lys Gly Arg Val Leu Thr Pro His Ala Asp Tyr 145 150 155 160 tgt cta ccc gga att aca cgt gcc aca gtg atc gat ctt gcc cgt aag 528 Cys Leu Pro Gly Ile Thr Arg Ala Thr Val Ile Asp Leu Ala Arg Lys 165 170 175 gag gga ctt gc 539 Glu Gly Leu 42 179 PRT Physcomitrella patens 42 Glu Glu His Leu Asp Arg Leu Phe Asp Ser Ala Lys Ala Met Ala Phe 1 5 10 15 Ala Asn Val Pro Ser Arg Ser Glu Val Lys Arg Ala Leu Phe Ala Thr 20 25 30 Leu Ile Ala Asn Asn Met Arg Asp Asn Ala His Val Arg Leu Thr Leu 35 40 45 Thr Arg Gly Glu Lys Thr Thr Ser Gly Met Ser Pro Ala Phe Asn Val 50 55 60 Tyr Gly Cys Asn Leu Ile Val Leu Ala Glu Trp Lys Pro Pro Val Tyr 65 70 75 80 Asn Asn Thr Asp Gly Ile Cys Leu Ile Thr Ala Ser Thr Arg Arg Asn 85 90 95 Ser Pro Asn Ser Leu Asn Ser Lys Ile His His Asn Asn Leu Ile Asn 100 105 110 Asn Ile Leu Ala Lys Val Glu Gly Asn Leu Ala Gly Ala Gly Asp Ala 115 120 125 Leu Met Leu Asp Cys Asp Gly Phe Val Ser Glu Thr Asn Ala Thr Asn 130 135 140 Ile Phe Met Val Lys Lys Gly Arg Val Leu Thr Pro His Ala Asp Tyr 145 150 155 160 Cys Leu Pro Gly Ile Thr Arg Ala Thr Val Ile Asp Leu Ala Arg Lys 165 170 175 Glu Gly Leu 43 560 DNA Physcomitrella patens CDS (3)..(560) 85_bd02_g04rev 43 tt cgt cgg tgt gga gac tcc ggg ccc ctc aat ttt gac ctt cac tcg 47 Arg Arg Cys Gly Asp Ser Gly Pro Leu Asn Phe Asp Leu His Ser 1 5 10 15 caa tcc tgc cat ttt cca tgc tgt cga ttg atc acg tca tct gaa gca 95 Gln Ser Cys His Phe Pro Cys Cys Arg Leu Ile Thr Ser Ser Glu Ala 20 25 30 aca atg tgg agg aat tcg agg aat ttg agg gac att tac agc aag ttg 143 Thr Met Trp Arg Asn Ser Arg Asn Leu Arg Asp Ile Tyr Ser Lys Leu 35 40 45 tcg aga tgc gtg gaa agg cgg tcc atg agc aac ctg cct gag agc acg 191 Ser Arg Cys Val Glu Arg Arg Ser Met Ser Asn Leu Pro Glu Ser Thr 50 55 60 gta tat gga ggc ccc aag tcc aag tcg ccg tgg aaa agg gtg acg ttg 239 Val Tyr Gly Gly Pro Lys Ser Lys Ser Pro Trp Lys Arg Val Thr Leu 65 70 75 cgg cac ctt gaa gcc aag tat caa acg aat cag ccc atc acg atg gta 287 Arg His Leu Glu Ala Lys Tyr Gln Thr Asn Gln Pro Ile Thr Met Val 80 85 90 95 act gcg tat gat tat ccc tcc ggg gcg cat gtg gat cga gca ggc ata 335 Thr Ala Tyr Asp Tyr Pro Ser Gly Ala His Val Asp Arg Ala Gly Ile 100 105 110 gac ata tgt ctg gta ggg gac tca gtg ggt atg gtt gtg cat ggg cat 383 Asp Ile Cys Leu Val Gly Asp Ser Val Gly Met Val Val His Gly His 115 120 125 gac aca acg ctg cca gtc aca atg gag gac atg ctg ctg cat tgc aag 431 Asp Thr Thr Leu Pro Val Thr Met Glu Asp Met Leu Leu His Cys Lys 130 135 140 gcg gta gca agg ggc gca gat cga cct ctt ctg gtt gga gat ttg cca 479 Ala Val Ala Arg Gly Ala Asp Arg Pro Leu Leu Val Gly Asp Leu Pro 145 150 155 ttt ggg agc tat gag cag agc aca cag cag gca gta gca agt gcg aca 527 Phe Gly Ser Tyr Glu Gln Ser Thr Gln Gln Ala Val Ala Ser Ala Thr 160 165 170 175 cgg atg ctc aag gag ggt gga atg gat gca gta 560 Arg Met Leu Lys Glu Gly Gly Met Asp Ala Val 180 185 44 186 PRT Physcomitrella patens 44 Arg Arg Cys Gly Asp Ser Gly Pro Leu Asn Phe Asp Leu His Ser Gln 1 5 10 15 Ser Cys His Phe Pro Cys Cys Arg Leu Ile Thr Ser Ser Glu Ala Thr 20 25 30 Met Trp Arg Asn Ser Arg Asn Leu Arg Asp Ile Tyr Ser Lys Leu Ser 35 40 45 Arg Cys Val Glu Arg Arg Ser Met Ser Asn Leu Pro Glu Ser Thr Val 50 55 60 Tyr Gly Gly Pro Lys Ser Lys Ser Pro Trp Lys Arg Val Thr Leu Arg 65 70 75 80 His Leu Glu Ala Lys Tyr Gln Thr Asn Gln Pro Ile Thr Met Val Thr 85 90 95 Ala Tyr Asp Tyr Pro Ser Gly Ala His Val Asp Arg Ala Gly Ile Asp 100 105 110 Ile Cys Leu Val Gly Asp Ser Val Gly Met Val Val His Gly His Asp 115 120 125 Thr Thr Leu Pro Val Thr Met Glu Asp Met Leu Leu His Cys Lys Ala 130 135 140 Val Ala Arg Gly Ala Asp Arg Pro Leu Leu Val Gly Asp Leu Pro Phe 145 150 155 160 Gly Ser Tyr Glu Gln Ser Thr Gln Gln Ala Val Ala Ser Ala Thr Arg 165 170 175 Met Leu Lys Glu Gly Gly Met Asp Ala Val 180 185 45 549 DNA Physcomitrella patens CDS (2)..(547) 85_ppprot1_083_g04 45 t gga gtt gca cgt atc aat aat ggg tcc ttc gga agt gcc ccg aag tgc 49 Gly Val Ala Arg Ile Asn Asn Gly Ser Phe Gly Ser Ala Pro Lys Cys 1 5 10 15 gtg ctg gac gat caa gca gaa tgg aaa gcc caa tgg cta cga cat ccc 97 Val Leu Asp Asp Gln Ala Glu Trp Lys Ala Gln Trp Leu Arg His Pro 20 25 30 gac gcc ttt tgc tgg gat ccc ctc acg gat ggt ttc ttg gct gcc agg 145 Asp Ala Phe Cys Trp Asp Pro Leu Thr Asp Gly Phe Leu Ala Ala Arg 35 40 45 aaa gga ttg gcg gaa ttg atc ggc tat ccg gat gtg gac gag gtt gtg 193 Lys Gly Leu Ala Glu Leu Ile Gly Tyr Pro Asp Val Asp Glu Val Val 50 55 60 ttg ctg gaa aac gct acc tca ggc gcg gcg att gtg gct ctg gat tgc 241 Leu Leu Glu Asn Ala Thr Ser Gly Ala Ala Ile Val Ala Leu Asp Cys 65 70 75 80 atg tgg gga ttc ctg gag gga agg ttt caa cag ggc gat gcc att ttg 289 Met Trp Gly Phe Leu Glu Gly Arg Phe Gln Gln Gly Asp Ala Ile Leu 85 90 95 atg ttc gat tcc gcc tat ggc gct gtg aag aag tgc ttc cag gcc tac 337 Met Phe Asp Ser Ala Tyr Gly Ala Val Lys Lys Cys Phe Gln Ala Tyr 100 105 110 tgt gta cgc gct ggc gcg cat ctg ctc gaa tac aaa atg cct ttc ccg 385 Cys Val Arg Ala Gly Ala His Leu Leu Glu Tyr Lys Met Pro Phe Pro 115 120 125 gtc gca tct aat tct gaa att att cgc acc ttc gaa gag ttt ctt cag 433 Val Ala Ser Asn Ser Glu Ile Ile Arg Thr Phe Glu Glu Phe Leu Gln 130 135 140 aag aaa aag gca gag tat cca tct cgc acg atc cga ctc gtc atc ctg 481 Lys Lys Lys Ala Glu Tyr Pro Ser Arg Thr Ile Arg Leu Val Ile Leu 145 150 155 160 gac cac ata act tca atg ccg tcc atc att ctt ccc gtc cga gat ctt 529 Asp His Ile Thr Ser Met Pro Ser Ile Ile Leu Pro Val Arg Asp Leu 165 170 175 gtt tgt tta tgt cca att ac 549 Val Cys Leu Cys Pro Ile 180 46 182 PRT Physcomitrella patens 46 Gly Val Ala Arg Ile Asn Asn Gly Ser Phe Gly Ser Ala Pro Lys Cys 1 5 10 15 Val Leu Asp Asp Gln Ala Glu Trp Lys Ala Gln Trp Leu Arg His Pro 20 25 30 Asp Ala Phe Cys Trp Asp Pro Leu Thr Asp Gly Phe Leu Ala Ala Arg 35 40 45 Lys Gly Leu Ala Glu Leu Ile Gly Tyr Pro Asp Val Asp Glu Val Val 50 55 60 Leu Leu Glu Asn Ala Thr Ser Gly Ala Ala Ile Val Ala Leu Asp Cys 65 70 75 80 Met Trp Gly Phe Leu Glu Gly Arg Phe Gln Gln Gly Asp Ala Ile Leu 85 90 95 Met Phe Asp Ser Ala Tyr Gly Ala Val Lys Lys Cys Phe Gln Ala Tyr 100 105 110 Cys Val Arg Ala Gly Ala His Leu Leu Glu Tyr Lys Met Pro Phe Pro 115 120 125 Val Ala Ser Asn Ser Glu Ile Ile Arg Thr Phe Glu Glu Phe Leu Gln 130 135 140 Lys Lys Lys Ala Glu Tyr Pro Ser Arg Thr Ile Arg Leu Val Ile Leu 145 150 155 160 Asp His Ile Thr Ser Met Pro Ser Ile Ile Leu Pro Val Arg Asp Leu 165 170 175 Val Cys Leu Cys Pro Ile 180 47 637 DNA Physcomitrella patens CDS (274)..(636) 45_ppprot1_093_h02 47 ttttttttta aaacaatcgt ggaattcatt taagattcat tctccaaccc atcttcttct 60 cctctattcc catgtttgga gactagaaat gcccaccatg gttggtatca tagccaaagg 120 ggcacacaca ggaagcccac tcctaaggtc catgaaaaac cagttattat atgtagaaag 180 gaacaagttc tgaagaaaca ttttgtgccg ctagttgtga gtcaaaaccg ctagttttag 240 agggagtgaa agcgcttttc tacatgaccg tag ctc gag cca ctc aca gta atc 294 Leu Glu Pro Leu Thr Val Ile 1 5 tac atc gag cgt gga gac gct aga aat gac gtc gga ggt ggg tca ttt 342 Tyr Ile Glu Arg Gly Asp Ala Arg Asn Asp Val Gly Gly Gly Ser Phe 10 15 20 gag gga gag ctt ttg gcg aag gac gtc cat aat gga gtc cag atc gtc 390 Glu Gly Glu Leu Leu Ala Lys Asp Val His Asn Gly Val Gln Ile Val 25 30 35 agc cac cga gat ggg agg att agc aaa ctg gct tgt gat tgc tgg cag 438 Ser His Arg Asp Gly Arg Ile Ser Lys Leu Ala Cys Asp Cys Trp Gln 40 45 50 55 ccc aga aga atg ata ctc gac ttt aga ttg ggt gaa ttt gag tcc gtg 486 Pro Arg Arg Met Ile Leu Asp Phe Arg Leu Gly Glu Phe Glu Ser Val 60 65 70 agc ggt gct tac gac gac tgt cct gtc gtt gcg acc gat gac gcc acg 534 Ser Gly Ala Tyr Asp Asp Cys Pro Val Val Ala Thr Asp Asp Ala Thr 75 80 85 ctg cct cag ttt ctg caa agc aac cag agc aac gcc tgt gtg agg gca 582 Leu Pro Gln Phe Leu Gln Ser Asn Gln Ser Asn Ala Cys Val Arg Ala 90 95 100 agt gaa cat tcc aga ctt gtc tgc ttg agc aca tgc atc cat gat ctc 630 Ser Glu His Ser Arg Leu Val Cys Leu Ser Thr Cys Ile His Asp Leu 105 110 115 ttg ctc c 637 Leu Leu 120 48 121 PRT Physcomitrella patens 48 Leu Glu Pro Leu Thr Val Ile Tyr Ile Glu Arg Gly Asp Ala Arg Asn 1 5 10 15 Asp Val Gly Gly Gly Ser Phe Glu Gly Glu Leu Leu Ala Lys Asp Val 20 25 30 His Asn Gly Val Gln Ile Val Ser His Arg Asp Gly Arg Ile Ser Lys 35 40 45 Leu Ala Cys Asp Cys Trp Gln Pro Arg Arg Met Ile Leu Asp Phe Arg 50 55 60 Leu Gly Glu Phe Glu Ser Val Ser Gly Ala Tyr Asp Asp Cys Pro Val 65 70 75 80 Val Ala Thr Asp Asp Ala Thr Leu Pro Gln Phe Leu Gln Ser Asn Gln 85 90 95 Ser Asn Ala Cys Val Arg Ala Ser Glu His Ser Arg Leu Val Cys Leu 100 105 110 Ser Thr Cys Ile His Asp Leu Leu Leu 115 120 49 492 DNA Physcomitrella patens CDS (3)..(491) 42_ppprot1 49 ta gaa gat ttt ggt tgt gag ggg gtt tgt ggg tct tgt cgt att gtg 47 Glu Asp Phe Gly Cys Glu Gly Val Cys Gly Ser Cys Arg Ile Val 1 5 10 15 ccg cag agg agt cga aga gag cga gcg agc gag gag gag aga ccg gag 95 Pro Gln Arg Ser Arg Arg Glu Arg Ala Ser Glu Glu Glu Arg Pro Glu 20 25 30 gga gag atg gga cgg aag gag ggt gtg att gcg ctc ttc gat gtg gat 143 Gly Glu Met Gly Arg Lys Glu Gly Val Ile Ala Leu Phe Asp Val Asp 35 40 45 ggc acc ctc acg cct cct cgg aag gag gtg tca gcg gac atg ctc cag 191 Gly Thr Leu Thr Pro Pro Arg Lys Glu Val Ser Ala Asp Met Leu Gln 50 55 60 ttt ctc cag gac tta cgt cag gtg gtc acc ata ggt gtt gtg gga ggt 239 Phe Leu Gln Asp Leu Arg Gln Val Val Thr Ile Gly Val Val Gly Gly 65 70 75 tcg gat ctc gtc aag atc tca gaa caa ctt ggg aaa act gct gtt acg 287 Ser Asp Leu Val Lys Ile Ser Glu Gln Leu Gly Lys Thr Ala Val Thr 80 85 90 95 gat tac gac tac gtt ttt tct gag aat ggg ttg gtt gcc cac aag gcg 335 Asp Tyr Asp Tyr Val Phe Ser Glu Asn Gly Leu Val Ala His Lys Ala 100 105 110 gga aag ctt atc gga agc cag agt ctg aag tca cac ttg gga gag gca 383 Gly Lys Leu Ile Gly Ser Gln Ser Leu Lys Ser His Leu Gly Glu Ala 115 120 125 aag ttg aaa gaa ttc atc aac ttt gtg ctt cac tac att gct gat ctt 431 Lys Leu Lys Glu Phe Ile Asn Phe Val Leu His Tyr Ile Ala Asp Leu 130 135 140 gat atc ccc att aag agg gga act ttc gtc gag ttt cgc atg ggt atg 479 Asp Ile Pro Ile Lys Arg Gly Thr Phe Val Glu Phe Arg Met Gly Met 145 150 155 ctc aat gtt tct c 492 Leu Asn Val Ser 160 50 163 PRT Physcomitrella patens 50 Glu Asp Phe Gly Cys Glu Gly Val Cys Gly Ser Cys Arg Ile Val Pro 1 5 10 15 Gln Arg Ser Arg Arg Glu Arg Ala Ser Glu Glu Glu Arg Pro Glu Gly 20 25 30 Glu Met Gly Arg Lys Glu Gly Val Ile Ala Leu Phe Asp Val Asp Gly 35 40 45 Thr Leu Thr Pro Pro Arg Lys Glu Val Ser Ala Asp Met Leu Gln Phe 50 55 60 Leu Gln Asp Leu Arg Gln Val Val Thr Ile Gly Val Val Gly Gly Ser 65 70 75 80 Asp Leu Val Lys Ile Ser Glu Gln Leu Gly Lys Thr Ala Val Thr Asp 85 90 95 Tyr Asp Tyr Val Phe Ser Glu Asn Gly Leu Val Ala His Lys Ala Gly 100 105 110 Lys Leu Ile Gly Ser Gln Ser Leu Lys Ser His Leu Gly Glu Ala Lys 115 120 125 Leu Lys Glu Phe Ile Asn Phe Val Leu His Tyr Ile Ala Asp Leu Asp 130 135 140 Ile Pro Ile Lys Arg Gly Thr Phe Val Glu Phe Arg Met Gly Met Leu 145 150 155 160 Asn Val Ser 51 338 DNA Physcomitrella patens CDS (161)..(331) 05_ck3_a03fwd 51 gttaaattaa atatttgaaa catgcctgga attctttctg gggggcgatt ttgacgggtt 60 ctgtctttga gaaaatcaac aaatatgtac atttccttga ttgttagtca ctcgagtatc 120 tagttccctt cgcgttatgt tcatttatag actcgcatag gtt ctc ggg cat aat 175 Val Leu Gly His Asn 1 5 gca cgt gca tgt cat ctt ggc ttt acg tac cac tca gca tta cga tct 223 Ala Arg Ala Cys His Leu Gly Phe Thr Tyr His Ser Ala Leu Arg Ser 10 15 20 gat tgg aag aaa atc ttg cag gaa aat gct gta gtg atg cac tct ata 271 Asp Trp Lys Lys Ile Leu Gln Glu Asn Ala Val Val Met His Ser Ile 25 30 35 gtt ggc tgg aag tct aca ttg ggc aaa tgg gct cga gtt cag gca aga 319 Val Gly Trp Lys Ser Thr Leu Gly Lys Trp Ala Arg Val Gln Ala Arg 40 45 50 att atc cta ttt tgatacc 338 Ile Ile Leu Phe 55 52 57 PRT Physcomitrella patens 52 Val Leu Gly His Asn Ala Arg Ala Cys His Leu Gly Phe Thr Tyr His 1 5 10 15 Ser Ala Leu Arg Ser Asp Trp Lys Lys Ile Leu Gln Glu Asn Ala Val 20 25 30 Val Met His Ser Ile Val Gly Trp Lys Ser Thr Leu Gly Lys Trp Ala 35 40 45 Arg Val Gln Ala Arg Ile Ile Leu Phe 50 55 53 579 DNA Physcomitrella patens CDS (52)..(579) 56_ppprot1_105_b10 53 ccggagtgct gtctgatact cttcgcgtgt cgtcggagct tgtgaatcag a atg gcg 57 Met Ala 1 aag tct tac cca aac gtc agt gag aag tac gct gcg ctc att gag aaa 105 Lys Ser Tyr Pro Asn Val Ser Glu Lys Tyr Ala Ala Leu Ile Glu Lys 5 10 15 gcc cgc agg aag ata cgg ggg atg gta gca gag aag aac tgc gca ccg 153 Ala Arg Arg Lys Ile Arg Gly Met Val Ala Glu Lys Asn Cys Ala Pro 20 25 30 atc atc ctt cgt ctc gca tgg cac ggg tcg gga act tac gat cag gag 201 Ile Ile Leu Arg Leu Ala Trp His Gly Ser Gly Thr Tyr Asp Gln Glu 35 40 45 50 tcg aag aca gga ggt cct ctt gga acc atc cgg ttc ggg cag gag ctt 249 Ser Lys Thr Gly Gly Pro Leu Gly Thr Ile Arg Phe Gly Gln Glu Leu 55 60 65 gcg cac ggc gcc aac gcg ggg ctg gac att gca gtg aat ctg ctg cag 297 Ala His Gly Ala Asn Ala Gly Leu Asp Ile Ala Val Asn Leu Leu Gln 70 75 80 ccc atc aag gag cag ttt ccg gag ttg tcg tac gct gac ttt tac acg 345 Pro Ile Lys Glu Gln Phe Pro Glu Leu Ser Tyr Ala Asp Phe Tyr Thr 85 90 95 ctg gct gga gtc gtt gcc gtg gag gtg aca ggc ggg ccc acc att cct 393 Leu Ala Gly Val Val Ala Val Glu Val Thr Gly Gly Pro Thr Ile Pro 100 105 110 ttt cac cct ggg cgc aag gat cat gag aca tgc ccc gtg gag ggt cgg 441 Phe His Pro Gly Arg Lys Asp His Glu Thr Cys Pro Val Glu Gly Arg 115 120 125 130 ctt ccc gac gcc acg aag ggt ttg gat cac ctc cga tgc gtg ttc acg 489 Leu Pro Asp Ala Thr Lys Gly Leu Asp His Leu Arg Cys Val Phe Thr 135 140 145 aag cag atg ggg ttg acg gat aaa gac att gtg gtg ctg tcg ggt gca 537 Lys Gln Met Gly Leu Thr Asp Lys Asp Ile Val Val Leu Ser Gly Ala 150 155 160 cac act ctg ggg agg tgc cac aag gac cgg tcc gga ttt gag 579 His Thr Leu Gly Arg Cys His Lys Asp Arg Ser Gly Phe Glu 165 170 175 54 176 PRT Physcomitrella patens 54 Met Ala Lys Ser Tyr Pro Asn Val Ser Glu Lys Tyr Ala Ala Leu Ile 1 5 10 15 Glu Lys Ala Arg Arg Lys Ile Arg Gly Met Val Ala Glu Lys Asn Cys 20 25 30 Ala Pro Ile Ile Leu Arg Leu Ala Trp His Gly Ser Gly Thr Tyr Asp 35 40 45 Gln Glu Ser Lys Thr Gly Gly Pro Leu Gly Thr Ile Arg Phe Gly Gln 50 55 60 Glu Leu Ala His Gly Ala Asn Ala Gly Leu Asp Ile Ala Val Asn Leu 65 70 75 80 Leu Gln Pro Ile Lys Glu Gln Phe Pro Glu Leu Ser Tyr Ala Asp Phe 85 90 95 Tyr Thr Leu Ala Gly Val Val Ala Val Glu Val Thr Gly Gly Pro Thr 100 105 110 Ile Pro Phe His Pro Gly Arg Lys Asp His Glu Thr Cys Pro Val Glu 115 120 125 Gly Arg Leu Pro Asp Ala Thr Lys Gly Leu Asp His Leu Arg Cys Val 130 135 140 Phe Thr Lys Gln Met Gly Leu Thr Asp Lys Asp Ile Val Val Leu Ser 145 150 155 160 Gly Ala His Thr Leu Gly Arg Cys His Lys Asp Arg Ser Gly Phe Glu 165 170 175 55 366 DNA Physcomitrella patens CDS (1)..(366) 87_ppprot135_g05 55 gtg gtg tcg tcg tgc ggg cac gac ggg cca ttc ggg gcg acc ggg gtg 48 Val Val Ser Ser Cys Gly His Asp Gly Pro Phe Gly Ala Thr Gly Val 1 5 10 15 aag cgg ctg cgg agc atc ggg atg atc gag agc gtg ccg ggg atg aag 96 Lys Arg Leu Arg Ser Ile Gly Met Ile Glu Ser Val Pro Gly Met Lys 20 25 30 tgc ctg gac atg aac gcg gcg gag gac gcg att gtg aag cac acg cgg 144 Cys Leu Asp Met Asn Ala Ala Glu Asp Ala Ile Val Lys His Thr Arg 35 40 45 gag gtg gtg cca ggg atg atc gtg acg ggc atg gag gtg gcg gag atc 192 Glu Val Val Pro Gly Met Ile Val Thr Gly Met Glu Val Ala Glu Ile 50 55 60 gac ggg tcg ccg aga atg gga ccc aca ttc gga gcg atg atg ata tcc 240 Asp Gly Ser Pro Arg Met Gly Pro Thr Phe Gly Ala Met Met Ile Ser 65 70 75 80 ggg cag aag gcg gca cac ttg gcg ctg agg gcg ttg ggg cta ccc aac 288 Gly Gln Lys Ala Ala His Leu Ala Leu Arg Ala Leu Gly Leu Pro Asn 85 90 95 gag gtg gac ggg aac tac aag ccc aat gtg cac cca gag ctg gta ttg 336 Glu Val Asp Gly Asn Tyr Lys Pro Asn Val His Pro Glu Leu Val Leu 100 105 110 gcg tcc acc gac gac atg acg gca tcc gct 366 Ala Ser Thr Asp Asp Met Thr Ala Ser Ala 115 120 56 122 PRT Physcomitrella patens 56 Val Val Ser Ser Cys Gly His Asp Gly Pro Phe Gly Ala Thr Gly Val 1 5 10 15 Lys Arg Leu Arg Ser Ile Gly Met Ile Glu Ser Val Pro Gly Met Lys 20 25 30 Cys Leu Asp Met Asn Ala Ala Glu Asp Ala Ile Val Lys His Thr Arg 35 40 45 Glu Val Val Pro Gly Met Ile Val Thr Gly Met Glu Val Ala Glu Ile 50 55 60 Asp Gly Ser Pro Arg Met Gly Pro Thr Phe Gly Ala Met Met Ile Ser 65 70 75 80 Gly Gln Lys Ala Ala His Leu Ala Leu Arg Ala Leu Gly Leu Pro Asn 85 90 95 Glu Val Asp Gly Asn Tyr Lys Pro Asn Val His Pro Glu Leu Val Leu 100 105 110 Ala Ser Thr Asp Asp Met Thr Ala Ser Ala 115 120 57 378 DNA Physcomitrella patens CDS (1)..(378) 47_mm13_h03rev 57 acg agc gag atg acc cgg cgc tac atg acc gac atg atc acc cac gcc 48 Thr Ser Glu Met Thr Arg Arg Tyr Met Thr Asp Met Ile Thr His Ala 1 5 10 15 gac acc gac gtg gtg gtg gtg ggt gct ggg tcc gcg ggg ctg tcg tgc 96 Asp Thr Asp Val Val Val Val Gly Ala Gly Ser Ala Gly Leu Ser Cys 20 25 30 gcg tac gag ctg tcc aag aac ccc aac gtg aag gtg gcc atc gtg gag 144 Ala Tyr Glu Leu Ser Lys Asn Pro Asn Val Lys Val Ala Ile Val Glu 35 40 45 cag tcg gtg tcg cct gga gga ggc gcg tgg tta ggc ggg caa ttg ttc 192 Gln Ser Val Ser Pro Gly Gly Gly Ala Trp Leu Gly Gly Gln Leu Phe 50 55 60 tcg gcc atg atc gta cgc aag ccg gcg cac cgg ttc ctg gac gag atc 240 Ser Ala Met Ile Val Arg Lys Pro Ala His Arg Phe Leu Asp Glu Ile 65 70 75 80 gag gtg ccg tac gag gag atg gag aac tac gtg gtg atc aag cac gcg 288 Glu Val Pro Tyr Glu Glu Met Glu Asn Tyr Val Val Ile Lys His Ala 85 90 95 gcg ctg ttc acg tcc acg atc atg agc aag ctg ctg gcg cgg ccg aac 336 Ala Leu Phe Thr Ser Thr Ile Met Ser Lys Leu Leu Ala Arg Pro Asn 100 105 110 gtg aag ctg ttc aac gcg gtg gcg gcg gag gat ctg att atc 378 Val Lys Leu Phe Asn Ala Val Ala Ala Glu Asp Leu Ile Ile 115 120 125 58 126 PRT Physcomitrella patens 58 Thr Ser Glu Met Thr Arg Arg Tyr Met Thr Asp Met Ile Thr His Ala 1 5 10 15 Asp Thr Asp Val Val Val Val Gly Ala Gly Ser Ala Gly Leu Ser Cys 20 25 30 Ala Tyr Glu Leu Ser Lys Asn Pro Asn Val Lys Val Ala Ile Val Glu 35 40 45 Gln Ser Val Ser Pro Gly Gly Gly Ala Trp Leu Gly Gly Gln Leu Phe 50 55 60 Ser Ala Met Ile Val Arg Lys Pro Ala His Arg Phe Leu Asp Glu Ile 65 70 75 80 Glu Val Pro Tyr Glu Glu Met Glu Asn Tyr Val Val Ile Lys His Ala 85 90 95 Ala Leu Phe Thr Ser Thr Ile Met Ser Lys Leu Leu Ala Arg Pro Asn 100 105 110 Val Lys Leu Phe Asn Ala Val Ala Ala Glu Asp Leu Ile Ile 115 120 125 59 452 DNA Physcomitrella patens CDS (2)..(265) 47_ppprot1_093_h03 59 g caa atc gaa act tac aca aga caa gga ttc acg gat ttg ccc atc tgt 49 Gln Ile Glu Thr Tyr Thr Arg Gln Gly Phe Thr Asp Leu Pro Ile Cys 1 5 10 15 atg gca aag aca caa tac tcc ttt tca gac aat gca gct gca aag ggt 97 Met Ala Lys Thr Gln Tyr Ser Phe Ser Asp Asn Ala Ala Ala Lys Gly 20 25 30 gta ccg acg gga ttc acc ctg ccc atc cga gat gtc aga gcc agt gtg 145 Val Pro Thr Gly Phe Thr Leu Pro Ile Arg Asp Val Arg Ala Ser Val 35 40 45 gga gca ggc ttt att tac cca att atc ggt aca atg agc aca atg ccc 193 Gly Ala Gly Phe Ile Tyr Pro Ile Ile Gly Thr Met Ser Thr Met Pro 50 55 60 ggg ctc ccg acc cga cct tgc ttc ttt gag att gac atg gac ctt gag 241 Gly Leu Pro Thr Arg Pro Cys Phe Phe Glu Ile Asp Met Asp Leu Glu 65 70 75 80 aca ggt atg gtt atg ggg cta tca tagatgttca gacacagacc ctgggttttg 295 Thr Gly Met Val Met Gly Leu Ser 85 acgctcaaag cgatcatgtt gattactaac atgtagtggt aaaattgtgt gctgagcata 355 tgatttaact ttggtgaatt gtgggcttgt tcaagtcgta tgtcttactt gttcgcactt 415 aataatattt ttttatactt aagttttgga aaaaaaa 452 60 88 PRT Physcomitrella patens 60 Gln Ile Glu Thr Tyr Thr Arg Gln Gly Phe Thr Asp Leu Pro Ile Cys 1 5 10 15 Met Ala Lys Thr Gln Tyr Ser Phe Ser Asp Asn Ala Ala Ala Lys Gly 20 25 30 Val Pro Thr Gly Phe Thr Leu Pro Ile Arg Asp Val Arg Ala Ser Val 35 40 45 Gly Ala Gly Phe Ile Tyr Pro Ile Ile Gly Thr Met Ser Thr Met Pro 50 55 60 Gly Leu Pro Thr Arg Pro Cys Phe Phe Glu Ile Asp Met Asp Leu Glu 65 70 75 80 Thr Gly Met Val Met Gly Leu Ser 85 61 574 DNA Physcomitrella patens CDS (1)..(573) 86_ppprot1_094_g10 61 gga gaa gtc att atc acc cag ctg ttt tat gat acc gat atc ttt ttg 48 Gly Glu Val Ile Ile Thr Gln Leu Phe Tyr Asp Thr Asp Ile Phe Leu 1 5 10 15 aaa ttt gtg aat gat tgt cgt caa att ggt atc aag gtg ccc att gta 96 Lys Phe Val Asn Asp Cys Arg Gln Ile Gly Ile Lys Val Pro Ile Val 20 25 30 cct ggt atc atg ccc att caa aat tac aag ggc ttt ctc cgc atg acc 144 Pro Gly Ile Met Pro Ile Gln Asn Tyr Lys Gly Phe Leu Arg Met Thr 35 40 45 acc ttg tgc aag acc aag gtg cca gct gaa atc atg gct gca cta gaa 192 Thr Leu Cys Lys Thr Lys Val Pro Ala Glu Ile Met Ala Ala Leu Glu 50 55 60 cct atc aaa gac aac gac gaa gca gtg aga gcg tat ggg atc cac cta 240 Pro Ile Lys Asp Asn Asp Glu Ala Val Arg Ala Tyr Gly Ile His Leu 65 70 75 80 ggc aca gaa atg tgc aag aag atc ctg gcg cat gac atc agg aca ttg 288 Gly Thr Glu Met Cys Lys Lys Ile Leu Ala His Asp Ile Arg Thr Leu 85 90 95 cac ttg tac tcc ttg aat ttg gag aaa tca gtt ctt ggc att tta cag 336 His Leu Tyr Ser Leu Asn Leu Glu Lys Ser Val Leu Gly Ile Leu Gln 100 105 110 aac ctg ggg ttg atc gac ttc agc agg gtt tct cgt cct cta ccg tgg 384 Asn Leu Gly Leu Ile Asp Phe Ser Arg Val Ser Arg Pro Leu Pro Trp 115 120 125 agg cct cca act aac agc aag cgt aca aag gag gac gtg cgt cct att 432 Arg Pro Pro Thr Asn Ser Lys Arg Thr Lys Glu Asp Val Arg Pro Ile 130 135 140 ttc tgg gcc aac cga cct aga agc tac att tca cga acc acc agc tgg 480 Phe Trp Ala Asn Arg Pro Arg Ser Tyr Ile Ser Arg Thr Thr Ser Trp 145 150 155 160 gac gat ttt cct cgt gga agg tgg gga gat acg cca acc ctg ctt acg 528 Asp Asp Phe Pro Arg Gly Arg Trp Gly Asp Thr Pro Thr Leu Leu Thr 165 170 175 gca gct tca gcg atc atc agt tca cca gga aga aga ccg tac caa g 574 Ala Ala Ser Ala Ile Ile Ser Ser Pro Gly Arg Arg Pro Tyr Gln 180 185 190 62 191 PRT Physcomitrella patens 62 Gly Glu Val Ile Ile Thr Gln Leu Phe Tyr Asp Thr Asp Ile Phe Leu 1 5 10 15 Lys Phe Val Asn Asp Cys Arg Gln Ile Gly Ile Lys Val Pro Ile Val 20 25 30 Pro Gly Ile Met Pro Ile Gln Asn Tyr Lys Gly Phe Leu Arg Met Thr 35 40 45 Thr Leu Cys Lys Thr Lys Val Pro Ala Glu Ile Met Ala Ala Leu Glu 50 55 60 Pro Ile Lys Asp Asn Asp Glu Ala Val Arg Ala Tyr Gly Ile His Leu 65 70 75 80 Gly Thr Glu Met Cys Lys Lys Ile Leu Ala His Asp Ile Arg Thr Leu 85 90 95 His Leu Tyr Ser Leu Asn Leu Glu Lys Ser Val Leu Gly Ile Leu Gln 100 105 110 Asn Leu Gly Leu Ile Asp Phe Ser Arg Val Ser Arg Pro Leu Pro Trp 115 120 125 Arg Pro Pro Thr Asn Ser Lys Arg Thr Lys Glu Asp Val Arg Pro Ile 130 135 140 Phe Trp Ala Asn Arg Pro Arg Ser Tyr Ile Ser Arg Thr Thr Ser Trp 145 150 155 160 Asp Asp Phe Pro Arg Gly Arg Trp Gly Asp Thr Pro Thr Leu Leu Thr 165 170 175 Ala Ala Ser Ala Ile Ile Ser Ser Pro Gly Arg Arg Pro Tyr Gln 180 185 190 63 409 DNA Physcomitrella patens CDS (2)..(409) 62_mm20_c10rev 63 t ggg att cag aac att ctt gct ctg cgt ggt gat cca cca cac ggc cag 49 Gly Ile Gln Asn Ile Leu Ala Leu Arg Gly Asp Pro Pro His Gly Gln 1 5 10 15 gac aaa ttc gta acc atc gaa gga ggg ttt tcc tgc gca tta gat ctg 97 Asp Lys Phe Val Thr Ile Glu Gly Gly Phe Ser Cys Ala Leu Asp Leu 20 25 30 gtg aga cac atc cga gcc aag tac ggt gat tat ttt gga att acc gtc 145 Val Arg His Ile Arg Ala Lys Tyr Gly Asp Tyr Phe Gly Ile Thr Val 35 40 45 gct gga tac cct gag gct cat cct gag gtg atc ggc gaa gac gga gtt 193 Ala Gly Tyr Pro Glu Ala His Pro Glu Val Ile Gly Glu Asp Gly Val 50 55 60 gca agc gag gag gcg tac cag aag gac ctg gct tat ctg aaa gaa aag 241 Ala Ser Glu Glu Ala Tyr Gln Lys Asp Leu Ala Tyr Leu Lys Glu Lys 65 70 75 80 tgt gac gca ggt gga gaa gtc att atc acc cag ctg ttt tat gat acc 289 Cys Asp Ala Gly Gly Glu Val Ile Ile Thr Gln Leu Phe Tyr Asp Thr 85 90 95 gat atc ttt ttg aaa ttt gtg aat gat tgt cgt caa att ggt atc aag 337 Asp Ile Phe Leu Lys Phe Val Asn Asp Cys Arg Gln Ile Gly Ile Lys 100 105 110 gtg ccc att gta cct ggt atc atg ccc att caa aat tac aag ggg ctt 385 Val Pro Ile Val Pro Gly Ile Met Pro Ile Gln Asn Tyr Lys Gly Leu 115 120 125 tct ccg cat gac cac ctt tgt gcc 409 Ser Pro His Asp His Leu Cys Ala 130 135 64 136 PRT Physcomitrella patens 64 Gly Ile Gln Asn Ile Leu Ala Leu Arg Gly Asp Pro Pro His Gly Gln 1 5 10 15 Asp Lys Phe Val Thr Ile Glu Gly Gly Phe Ser Cys Ala Leu Asp Leu 20 25 30 Val Arg His Ile Arg Ala Lys Tyr Gly Asp Tyr Phe Gly Ile Thr Val 35 40 45 Ala Gly Tyr Pro Glu Ala His Pro Glu Val Ile Gly Glu Asp Gly Val 50 55 60 Ala Ser Glu Glu Ala Tyr Gln Lys Asp Leu Ala Tyr Leu Lys Glu Lys 65 70 75 80 Cys Asp Ala Gly Gly Glu Val Ile Ile Thr Gln Leu Phe Tyr Asp Thr 85 90 95 Asp Ile Phe Leu Lys Phe Val Asn Asp Cys Arg Gln Ile Gly Ile Lys 100 105 110 Val Pro Ile Val Pro Gly Ile Met Pro Ile Gln Asn Tyr Lys Gly Leu 115 120 125 Ser Pro His Asp His Leu Cys Ala 130 135 65 450 DNA Physcomitrella patens CDS (3)..(449) 22_ck26_d08fwd 65 ga ctg gaa gcc act aca ata ccg gga aga ttt cag gtt gtt gag tca 47 Leu Glu Ala Thr Thr Ile Pro Gly Arg Phe Gln Val Val Glu Ser 1 5 10 15 gac agt tcc aag gca ctc ggt tgt ctt tct gcc agg ctc ata ctt gat 95 Asp Ser Ser Lys Ala Leu Gly Cys Leu Ser Ala Arg Leu Ile Leu Asp 20 25 30 gga gca cac aca gaa gac tct gcg ata gca ctt gca aag aca ctg cga 143 Gly Ala His Thr Glu Asp Ser Ala Ile Ala Leu Ala Lys Thr Leu Arg 35 40 45 gag ggt ttt ccc gat gca agt ttg gcg ttt gtt gta gca atg gct tct 191 Glu Gly Phe Pro Asp Ala Ser Leu Ala Phe Val Val Ala Met Ala Ser 50 55 60 gat aag gac gaa cac tct ttt gct cga att ttg ttg aca aag gcc aaa 239 Asp Lys Asp Glu His Ser Phe Ala Arg Ile Leu Leu Thr Lys Ala Lys 65 70 75 cct gac gtc gtg gtg acg aca aga gta cct gta gca ggg agc tac aat 287 Pro Asp Val Val Val Thr Thr Arg Val Pro Val Ala Gly Ser Tyr Asn 80 85 90 95 agg tgc cgt aca gca caa gag ctt gct gaa tgc tgg tcc caa acg gcc 335 Arg Cys Arg Thr Ala Gln Glu Leu Ala Glu Cys Trp Ser Gln Thr Ala 100 105 110 cag ggt ctg aat ctc cct tat cat ttt gag aca agc aaa caa aaa cta 383 Gln Gly Leu Asn Leu Pro Tyr His Phe Glu Thr Ser Lys Gln Lys Leu 115 120 125 cta caa gga ttt tct tct gtt gga tct tct gaa cat cag caa agt ggc 431 Leu Gln Gly Phe Ser Ser Val Gly Ser Ser Glu His Gln Gln Ser Gly 130 135 140 gct aag act tca agc aca g 450 Ala Lys Thr Ser Ser Thr 145 66 149 PRT Physcomitrella patens 66 Leu Glu Ala Thr Thr Ile Pro Gly Arg Phe Gln Val Val Glu Ser Asp 1 5 10 15 Ser Ser Lys Ala Leu Gly Cys Leu Ser Ala Arg Leu Ile Leu Asp Gly 20 25 30 Ala His Thr Glu Asp Ser Ala Ile Ala Leu Ala Lys Thr Leu Arg Glu 35 40 45 Gly Phe Pro Asp Ala Ser Leu Ala Phe Val Val Ala Met Ala Ser Asp 50 55 60 Lys Asp Glu His Ser Phe Ala Arg Ile Leu Leu Thr Lys Ala Lys Pro 65 70 75 80 Asp Val Val Val Thr Thr Arg Val Pro Val Ala Gly Ser Tyr Asn Arg 85 90 95 Cys Arg Thr Ala Gln Glu Leu Ala Glu Cys Trp Ser Gln Thr Ala Gln 100 105 110 Gly Leu Asn Leu Pro Tyr His Phe Glu Thr Ser Lys Gln Lys Leu Leu 115 120 125 Gln Gly Phe Ser Ser Val Gly Ser Ser Glu His Gln Gln Ser Gly Ala 130 135 140 Lys Thr Ser Ser Thr 145 67 581 DNA Physcomitrella patens CDS (74)..(493) 56_ck15_b10fwd 67 cttgcgctcc atcgccgcag ctgacccatt tgcccttctt cgcagggcgt gttggaattg 60 agcatctctg aca atg gct gac cag cgt tgc ccc agc gtg gtg agc aag 109 Met Ala Asp Gln Arg Cys Pro Ser Val Val Ser Lys 1 5 10 atg ggt gga aca tca tac ctg ggt tcc aga ttt aca cct agt cgt gcc 157 Met Gly Gly Thr Ser Tyr Leu Gly Ser Arg Phe Thr Pro Ser Arg Ala 15 20 25 atg tac ccc gcc tac gat ttc agc act cct ttc gcg gcc gct gcc aag 205 Met Tyr Pro Ala Tyr Asp Phe Ser Thr Pro Phe Ala Ala Ala Ala Lys 30 35 40 ctc ggt gct ctg ccc agg cag acg gga ttc aac tcc ccg tgc ccc atc 253 Leu Gly Ala Leu Pro Arg Gln Thr Gly Phe Asn Ser Pro Cys Pro Ile 45 50 55 60 gac gtg acc ggc ggg agg aac atg tcg agc cag gtg ttc gtt ccg gct 301 Asp Val Thr Gly Gly Arg Asn Met Ser Ser Gln Val Phe Val Pro Ala 65 70 75 gcg aat gaa aag aca ttc gct tcg ttc atg acc gac ttt ctg atg ggg 349 Ala Asn Glu Lys Thr Phe Ala Ser Phe Met Thr Asp Phe Leu Met Gly 80 85 90 ggt gtg tcg gcc gcg gta tct aag aca gca gct gcg ccc atc gag cgt 397 Gly Val Ser Ala Ala Val Ser Lys Thr Ala Ala Ala Pro Ile Glu Arg 95 100 105 gtg aag ctg ttg atc cag aac cag gac gaa atg ctg aag tcc ggg cgt 445 Val Lys Leu Leu Ile Gln Asn Gln Asp Glu Met Leu Lys Ser Gly Arg 110 115 120 ctg tct cac cct tac aag ggc att ggc gag tgc ttc agc ccg aac cat 493 Leu Ser His Pro Tyr Lys Gly Ile Gly Glu Cys Phe Ser Pro Asn His 125 130 135 140 taaggacgag ggaatgatgt cgctgtggcg tgggaacact gcgaatgtga tcagatactt 553 cccgacgcag ctttgaactt tgcattca 581 68 140 PRT Physcomitrella patens 68 Met Ala Asp Gln Arg Cys Pro Ser Val Val Ser Lys Met Gly Gly Thr 1 5 10 15 Ser Tyr Leu Gly Ser Arg Phe Thr Pro Ser Arg Ala Met Tyr Pro Ala 20 25 30 Tyr Asp Phe Ser Thr Pro Phe Ala Ala Ala Ala Lys Leu Gly Ala Leu 35 40 45 Pro Arg Gln Thr Gly Phe Asn Ser Pro Cys Pro Ile Asp Val Thr Gly 50 55 60 Gly Arg Asn Met Ser Ser Gln Val Phe Val Pro Ala Ala Asn Glu Lys 65 70 75 80 Thr Phe Ala Ser Phe Met Thr Asp Phe Leu Met Gly Gly Val Ser Ala 85 90 95 Ala Val Ser Lys Thr Ala Ala Ala Pro Ile Glu Arg Val Lys Leu Leu 100 105 110 Ile Gln Asn Gln Asp Glu Met Leu Lys Ser Gly Arg Leu Ser His Pro 115 120 125 Tyr Lys Gly Ile Gly Glu Cys Phe Ser Pro Asn His 130 135 140 69 533 DNA Physcomitrella patens CDS (3)..(533) 11_mm6 69 ga aaa tta act gaa gaa gtc gct gct tct gtg ggt aaa ttc ctg gct 47 Lys Leu Thr Glu Glu Val Ala Ala Ser Val Gly Lys Phe Leu Ala 1 5 10 15 gag aat caa act act gtg agc att ccc cct att gca caa acc cct gcg 95 Glu Asn Gln Thr Thr Val Ser Ile Pro Pro Ile Ala Gln Thr Pro Ala 20 25 30 aaa ttg aga cgg atg ccg ttc ggc gag agg gcg tcc cta tcc acg aac 143 Lys Leu Arg Arg Met Pro Phe Gly Glu Arg Ala Ser Leu Ser Thr Asn 35 40 45 cct acc ggg aag aag ctt ttc cag ttg atg gac agg aaa aag agc aac 191 Pro Thr Gly Lys Lys Leu Phe Gln Leu Met Asp Arg Lys Lys Ser Asn 50 55 60 ttg tcg gtt gcg gct gat gtg aat acg gcc agg gag ctt cta gcg ctg 239 Leu Ser Val Ala Ala Asp Val Asn Thr Ala Arg Glu Leu Leu Ala Leu 65 70 75 gct gag att gtt ggc cca gag atc tgt gtg ttg aaa acg cac gtt gac 287 Ala Glu Ile Val Gly Pro Glu Ile Cys Val Leu Lys Thr His Val Asp 80 85 90 95 atc ttg cca gac ttc acc cca gac ttc ggc agc aag ctt cgt gaa att 335 Ile Leu Pro Asp Phe Thr Pro Asp Phe Gly Ser Lys Leu Arg Glu Ile 100 105 110 gct gac aag cat gac ttt ttg atc ttt gag gat cgc aag ttt gca gac 383 Ala Asp Lys His Asp Phe Leu Ile Phe Glu Asp Arg Lys Phe Ala Asp 115 120 125 ata ggg aac acg gtg acc atg caa tac gag agt ggc att tac aag ata 431 Ile Gly Asn Thr Val Thr Met Gln Tyr Glu Ser Gly Ile Tyr Lys Ile 130 135 140 gtg gat tgg gcg gac atc acc aat gct cat gtt gtg cca ggt tca gga 479 Val Asp Trp Ala Asp Ile Thr Asn Ala His Val Val Pro Gly Ser Gly 145 150 155 att gtg gat ggt ttg aag ctg aag ggt ctg cct aag ggg cgc ggc ttt 527 Ile Val Asp Gly Leu Lys Leu Lys Gly Leu Pro Lys Gly Arg Gly Phe 160 165 170 175 tac ttc 533 Tyr Phe 70 177 PRT Physcomitrella patens 70 Lys Leu Thr Glu Glu Val Ala Ala Ser Val Gly Lys Phe Leu Ala Glu 1 5 10 15 Asn Gln Thr Thr Val Ser Ile Pro Pro Ile Ala Gln Thr Pro Ala Lys 20 25 30 Leu Arg Arg Met Pro Phe Gly Glu Arg Ala Ser Leu Ser Thr Asn Pro 35 40 45 Thr Gly Lys Lys Leu Phe Gln Leu Met Asp Arg Lys Lys Ser Asn Leu 50 55 60 Ser Val Ala Ala Asp Val Asn Thr Ala Arg Glu Leu Leu Ala Leu Ala 65 70 75 80 Glu Ile Val Gly Pro Glu Ile Cys Val Leu Lys Thr His Val Asp Ile 85 90 95 Leu Pro Asp Phe Thr Pro Asp Phe Gly Ser Lys Leu Arg Glu Ile Ala 100 105 110 Asp Lys His Asp Phe Leu Ile Phe Glu Asp Arg Lys Phe Ala Asp Ile 115 120 125 Gly Asn Thr Val Thr Met Gln Tyr Glu Ser Gly Ile Tyr Lys Ile Val 130 135 140 Asp Trp Ala Asp Ile Thr Asn Ala His Val Val Pro Gly Ser Gly Ile 145 150 155 160 Val Asp Gly Leu Lys Leu Lys Gly Leu Pro Lys Gly Arg Gly Phe Tyr 165 170 175 Phe 71 486 DNA Physcomitrella patens CDS (33)..(476) 13_ck25_c01fwd 71 gttttcgggg atatttcagc agttggggtt ga tcg aag cga ggc ctg agt gga 53 Ser Lys Arg Gly Leu Ser Gly 1 5 aag gag gag aaa gaa gga gag acg acg ccc atg gac gtg aaa gct gct 101 Lys Glu Glu Lys Glu Gly Glu Thr Thr Pro Met Asp Val Lys Ala Ala 10 15 20 ggc tca gtg gcg cag gac cag ttt tcc aag cat gca ggt cga agg aaa 149 Gly Ser Val Ala Gln Asp Gln Phe Ser Lys His Ala Gly Arg Arg Lys 25 30 35 gtt att atc gac acg gat ccc ggc att gat gat atg atg gca att tta 197 Val Ile Ile Asp Thr Asp Pro Gly Ile Asp Asp Met Met Ala Ile Leu 40 45 50 55 atg gct ttt caa gcc cct gaa att gaa gtt ata gga ctc acc acc att 245 Met Ala Phe Gln Ala Pro Glu Ile Glu Val Ile Gly Leu Thr Thr Ile 60 65 70 ttt ggc aac gta aac acc gat tta gcg aca atc aac gcc ctc cat ctg 293 Phe Gly Asn Val Asn Thr Asp Leu Ala Thr Ile Asn Ala Leu His Leu 75 80 85 tgc gag atg gca ggt cat ccg gag ata ccg gtt gcg gaa ggc cca tca 341 Cys Glu Met Ala Gly His Pro Glu Ile Pro Val Ala Glu Gly Pro Ser 90 95 100 gaa cca tta aag cgg gtg aag cct cga att gcg tat ttt gaa cac gga 389 Glu Pro Leu Lys Arg Val Lys Pro Arg Ile Ala Tyr Phe Glu His Gly 105 110 115 tca gat gga ctt gga gaa act tac caa gcc aaa cct aac ttc aaa agt 437 Ser Asp Gly Leu Gly Glu Thr Tyr Gln Ala Lys Pro Asn Phe Lys Ser 120 125 130 135 tat cta aag atg cag cag act ttc tta ttg aga atg taa ctgaattccc 486 Tyr Leu Lys Met Gln Gln Thr Phe Leu Leu Arg Met 140 145 72 147 PRT Physcomitrella patens 72 Ser Lys Arg Gly Leu Ser Gly Lys Glu Glu Lys Glu Gly Glu Thr Thr 1 5 10 15 Pro Met Asp Val Lys Ala Ala Gly Ser Val Ala Gln Asp Gln Phe Ser 20 25 30 Lys His Ala Gly Arg Arg Lys Val Ile Ile Asp Thr Asp Pro Gly Ile 35 40 45 Asp Asp Met Met Ala Ile Leu Met Ala Phe Gln Ala Pro Glu Ile Glu 50 55 60 Val Ile Gly Leu Thr Thr Ile Phe Gly Asn Val Asn Thr Asp Leu Ala 65 70 75 80 Thr Ile Asn Ala Leu His Leu Cys Glu Met Ala Gly His Pro Glu Ile 85 90 95 Pro Val Ala Glu Gly Pro Ser Glu Pro Leu Lys Arg Val Lys Pro Arg 100 105 110 Ile Ala Tyr Phe Glu His Gly Ser Asp Gly Leu Gly Glu Thr Tyr Gln 115 120 125 Ala Lys Pro Asn Phe Lys Ser Tyr Leu Lys Met Gln Gln Thr Phe Leu 130 135 140 Leu Arg Met 145 73 583 DNA Physcomitrella patens CDS (2)..(583) 42_ppprot1_075_g09 73 g ata aaa gcg gac gga ttg gca gcg ggg aaa ggt gta gtt gta gcg atg 49 Ile Lys Ala Asp Gly Leu Ala Ala Gly Lys Gly Val Val Val Ala Met 1 5 10 15 acg cta gag gaa gca tat gca gct gtg gat tcc atg ttg gtg agc agc 97 Thr Leu Glu Glu Ala Tyr Ala Ala Val Asp Ser Met Leu Val Ser Ser 20 25 30 gaa ttt gga tca gcg gga gga tta gtt ctt gtg gag gag ttt ctc gat 145 Glu Phe Gly Ser Ala Gly Gly Leu Val Leu Val Glu Glu Phe Leu Asp 35 40 45 ggt gag gag gtt tcg ttt ttt gca cta gta gac ggg gag aat gcg tta 193 Gly Glu Glu Val Ser Phe Phe Ala Leu Val Asp Gly Glu Asn Ala Leu 50 55 60 cca atg gca tca gcc caa gat cac aag cga gtc gga gat gga gac aca 241 Pro Met Ala Ser Ala Gln Asp His Lys Arg Val Gly Asp Gly Asp Thr 65 70 75 80 ggg ccg aac aca gga ggc atg gga gcc tat tcc ccc gcc ccg gct ctc 289 Gly Pro Asn Thr Gly Gly Met Gly Ala Tyr Ser Pro Ala Pro Ala Leu 85 90 95 act ccc gag att gag cag aag gtt atg gaa acc atc atc tac cct act 337 Thr Pro Glu Ile Glu Gln Lys Val Met Glu Thr Ile Ile Tyr Pro Thr 100 105 110 gtg aag ggc atg cgc gcc gaa gga tgt aaa tac ttg ggg gtt ctc tac 385 Val Lys Gly Met Arg Ala Glu Gly Cys Lys Tyr Leu Gly Val Leu Tyr 115 120 125 gca ggt gtg ata att gag aag aag aat ggc ttg ccg aag ctt ttg gag 433 Ala Gly Val Ile Ile Glu Lys Lys Asn Gly Leu Pro Lys Leu Leu Glu 130 135 140 tac aat gtg cgg ttc gga gac ccc gag tgc cag gtg ctc ttg att cgt 481 Tyr Asn Val Arg Phe Gly Asp Pro Glu Cys Gln Val Leu Leu Ile Arg 145 150 155 160 ctg cag tca gat ttg gtg caa gtt tta tta gca gca tgc aaa gga ggt 529 Leu Gln Ser Asp Leu Val Gln Val Leu Leu Ala Ala Cys Lys Gly Gly 165 170 175 ttg aat ggg gtc caa ctc gaa tgg act gaa gag cct gcc ctg gtg att 577 Leu Asn Gly Val Gln Leu Glu Trp Thr Glu Glu Pro Ala Leu Val Ile 180 185 190 gtt atg 583 Val Met 74 194 PRT Physcomitrella patens 74 Ile Lys Ala Asp Gly Leu Ala Ala Gly Lys Gly Val Val Val Ala Met 1 5 10 15 Thr Leu Glu Glu Ala Tyr Ala Ala Val Asp Ser Met Leu Val Ser Ser 20 25 30 Glu Phe Gly Ser Ala Gly Gly Leu Val Leu Val Glu Glu Phe Leu Asp 35 40 45 Gly Glu Glu Val Ser Phe Phe Ala Leu Val Asp Gly Glu Asn Ala Leu 50 55 60 Pro Met Ala Ser Ala Gln Asp His Lys Arg Val Gly Asp Gly Asp Thr 65 70 75 80 Gly Pro Asn Thr Gly Gly Met Gly Ala Tyr Ser Pro Ala Pro Ala Leu 85 90 95 Thr Pro Glu Ile Glu Gln Lys Val Met Glu Thr Ile Ile Tyr Pro Thr 100 105 110 Val Lys Gly Met Arg Ala Glu Gly Cys Lys Tyr Leu Gly Val Leu Tyr 115 120 125 Ala Gly Val Ile Ile Glu Lys Lys Asn Gly Leu Pro Lys Leu Leu Glu 130 135 140 Tyr Asn Val Arg Phe Gly Asp Pro Glu Cys Gln Val Leu Leu Ile Arg 145 150 155 160 Leu Gln Ser Asp Leu Val Gln Val Leu Leu Ala Ala Cys Lys Gly Gly 165 170 175 Leu Asn Gly Val Gln Leu Glu Trp Thr Glu Glu Pro Ala Leu Val Ile 180 185 190 Val Met 75 470 DNA Physcomitrella patens CDS (2)..(469) 44_ppprot3_003_h07 75 c acg gac ctc ttg att gct ccc gca ggt act aca ctg gaa gaa gcg act 49 Thr Asp Leu Leu Ile Ala Pro Ala Gly Thr Thr Leu Glu Glu Ala Thr 1 5 10 15 aaa att ctg act cga aac aag aag agt ttg cta ccc ctc gtt tcg gag 97 Lys Ile Leu Thr Arg Asn Lys Lys Ser Leu Leu Pro Leu Val Ser Glu 20 25 30 agc gga agc ttc gtc gag ctt ttg tgc cgg act gat ttg aag gct tac 145 Ser Gly Ser Phe Val Glu Leu Leu Cys Arg Thr Asp Leu Lys Ala Tyr 35 40 45 cat gcg ttg ccg cct att ggc gca cca tct ctt ggc tct gat gat aaa 193 His Ala Leu Pro Pro Ile Gly Ala Pro Ser Leu Gly Ser Asp Asp Lys 50 55 60 att ctt gtc ggc gct gca att ggt acc cgc gag agt gac aaa gac cgg 241 Ile Leu Val Gly Ala Ala Ile Gly Thr Arg Glu Ser Asp Lys Asp Arg 65 70 75 80 ttg aaa ctg ctt gtg gaa gct ggt gta aat gtt gtt att ctc gat agc 289 Leu Lys Leu Leu Val Glu Ala Gly Val Asn Val Val Ile Leu Asp Ser 85 90 95 tcg cag ggg gat tcc atg tac cag agg cag atg att gag tat atc aag 337 Ser Gln Gly Asp Ser Met Tyr Gln Arg Gln Met Ile Glu Tyr Ile Lys 100 105 110 aaa tca cat gct ggg ttg gat gtc atc gga gga aat gtt gtt act gcg 385 Lys Ser His Ala Gly Leu Asp Val Ile Gly Gly Asn Val Val Thr Ala 115 120 125 tac caa gcg aag aac ttg att gaa gcc ggt gtg gat ggg ttg cgg gtt 433 Tyr Gln Ala Lys Asn Leu Ile Glu Ala Gly Val Asp Gly Leu Arg Val 130 135 140 ggc atg ggc tct ggc tcc atc tgc aca acg caa gag g 470 Gly Met Gly Ser Gly Ser Ile Cys Thr Thr Gln Glu 145 150 155 76 156 PRT Physcomitrella patens 76 Thr Asp Leu Leu Ile Ala Pro Ala Gly Thr Thr Leu Glu Glu Ala Thr 1 5 10 15 Lys Ile Leu Thr Arg Asn Lys Lys Ser Leu Leu Pro Leu Val Ser Glu 20 25 30 Ser Gly Ser Phe Val Glu Leu Leu Cys Arg Thr Asp Leu Lys Ala Tyr 35 40 45 His Ala Leu Pro Pro Ile Gly Ala Pro Ser Leu Gly Ser Asp Asp Lys 50 55 60 Ile Leu Val Gly Ala Ala Ile Gly Thr Arg Glu Ser Asp Lys Asp Arg 65 70 75 80 Leu Lys Leu Leu Val Glu Ala Gly Val Asn Val Val Ile Leu Asp Ser 85 90 95 Ser Gln Gly Asp Ser Met Tyr Gln Arg Gln Met Ile Glu Tyr Ile Lys 100 105 110 Lys Ser His Ala Gly Leu Asp Val Ile Gly Gly Asn Val Val Thr Ala 115 120 125 Tyr Gln Ala Lys Asn Leu Ile Glu Ala Gly Val Asp Gly Leu Arg Val 130 135 140 Gly Met Gly Ser Gly Ser Ile Cys Thr Thr Gln Glu 145 150 155 77 554 DNA Physcomitrella patens CDS (1)..(552) 84_ppprot3_001_f12 77 tta ggg ttt aac agc agg ctc tca aat tcc att ctc tct ttc ctt tct 48 Leu Gly Phe Asn Ser Arg Leu Ser Asn Ser Ile Leu Ser Phe Leu Ser 1 5 10 15 ctg cgc ctt tgc ttt gcg ctt cta ctt gct gga cca ggg acc atg gct 96 Leu Arg Leu Cys Phe Ala Leu Leu Leu Ala Gly Pro Gly Thr Met Ala 20 25 30 atg gca gct gcc gca gct gtg gcc tcc cag ggc ctg gtt gca gca tca 144 Met Ala Ala Ala Ala Ala Val Ala Ser Gln Gly Leu Val Ala Ala Ser 35 40 45 acc cag cag cag aag aag acg tcc gcc aag ttg agc tgc aat gct gct 192 Thr Gln Gln Gln Lys Lys Thr Ser Ala Lys Leu Ser Cys Asn Ala Ala 50 55 60 cct gtg ttt tcg ggg aag agc ttt ctc agg gtg aag agc ggt agc aac 240 Pro Val Phe Ser Gly Lys Ser Phe Leu Arg Val Lys Ser Gly Ser Asn 65 70 75 80 ggc gca gtg aga gtg cgc aat gtt ggg gtg cgg tgc gag gcg cag gct 288 Gly Ala Val Arg Val Arg Asn Val Gly Val Arg Cys Glu Ala Gln Ala 85 90 95 att gag aga gag tct gtg aag gcg gac acg ggc tct ggt cgc gag gag 336 Ile Glu Arg Glu Ser Val Lys Ala Asp Thr Gly Ser Gly Arg Glu Glu 100 105 110 gac gca ttc agt ggg ctg aag cag gtg tgc gct gta ttg ggt acg cag 384 Asp Ala Phe Ser Gly Leu Lys Gln Val Cys Ala Val Leu Gly Thr Gln 115 120 125 tgg ggc gac gaa gga aag gga aaa ctt gtg gac atc tta gcc cag cgc 432 Trp Gly Asp Glu Gly Lys Gly Lys Leu Val Asp Ile Leu Ala Gln Arg 130 135 140 ttc gat gtt gtt gct cgt tgt cag ggg ggt gca aat gct ggt cac acg 480 Phe Asp Val Val Ala Arg Cys Gln Gly Gly Ala Asn Ala Gly His Thr 145 150 155 160 atc tac aac gac aag ggc gag aag ttt gca ctt cac ttg gta cct tca 528 Ile Tyr Asn Asp Lys Gly Glu Lys Phe Ala Leu His Leu Val Pro Ser 165 170 175 ggg atc ctt aat gag aaa acg acg tg 554 Gly Ile Leu Asn Glu Lys Thr Thr 180 78 184 PRT Physcomitrella patens 78 Leu Gly Phe Asn Ser Arg Leu Ser Asn Ser Ile Leu Ser Phe Leu Ser 1 5 10 15 Leu Arg Leu Cys Phe Ala Leu Leu Leu Ala Gly Pro Gly Thr Met Ala 20 25 30 Met Ala Ala Ala Ala Ala Val Ala Ser Gln Gly Leu Val Ala Ala Ser 35 40 45 Thr Gln Gln Gln Lys Lys Thr Ser Ala Lys Leu Ser Cys Asn Ala Ala 50 55 60 Pro Val Phe Ser Gly Lys Ser Phe Leu Arg Val Lys Ser Gly Ser Asn 65 70 75 80 Gly Ala Val Arg Val Arg Asn Val Gly Val Arg Cys Glu Ala Gln Ala 85 90 95 Ile Glu Arg Glu Ser Val Lys Ala Asp Thr Gly Ser Gly Arg Glu Glu 100 105 110 Asp Ala Phe Ser Gly Leu Lys Gln Val Cys Ala Val Leu Gly Thr Gln 115 120 125 Trp Gly Asp Glu Gly Lys Gly Lys Leu Val Asp Ile Leu Ala Gln Arg 130 135 140 Phe Asp Val Val Ala Arg Cys Gln Gly Gly Ala Asn Ala Gly His Thr 145 150 155 160 Ile Tyr Asn Asp Lys Gly Glu Lys Phe Ala Leu His Leu Val Pro Ser 165 170 175 Gly Ile Leu Asn Glu Lys Thr Thr 180 79 538 DNA Physcomitrella patens CDS (263)..(538) 77_ck14_e06fwd 79 cttaacacaa gaattttgac atatttacag ttcagacagc tgaaagcgac aagctgttta 60 cctggaagac ctacctaaaa ggtacatgac ccttaactaa ccaggagtgg aattaggact 120 aaaacgctaa atttcaagac gctactgaat gagccagtaa agattgactc catgatcaga 180 gctaagcagt cacagactgc gtcctacgat gccaaacatc cttttttaag gaaccatcgt 240 cgtgtcaaaa cctgccagct ga aaa ata gca aaa tgg agg cta aca aaa tgg 292 Lys Ile Ala Lys Trp Arg Leu Thr Lys Trp 1 5 10 tgt tcc aag aat aag aaa acc tac caa atg aca cat gtg gca act aca 340 Cys Ser Lys Asn Lys Lys Thr Tyr Gln Met Thr His Val Ala Thr Thr 15 20 25 caa tct ttc aga aaa aat gag cta agc atc aag gaa aga ctg ata gca 388 Gln Ser Phe Arg Lys Asn Glu Leu Ser Ile Lys Glu Arg Leu Ile Ala 30 35 40 tca ccc ttc ctc tca ccc cac aaa acc cta ttc aca agc caa ctt cgt 436 Ser Pro Phe Leu Ser Pro His Lys Thr Leu Phe Thr Ser Gln Leu Arg 45 50 55 atc aaa gct gct cag aca gat tgc aaa cgc ctg aaa agc gct caa agg 484 Ile Lys Ala Ala Gln Thr Asp Cys Lys Arg Leu Lys Ser Ala Gln Arg 60 65 70 gta ccg gta atc cat cgt aaa cat gtc ctt tcc gat ctt tcc gaa ctg 532 Val Pro Val Ile His Arg Lys His Val Leu Ser Asp Leu Ser Glu Leu 75 80 85 90 cag cag 538 Gln Gln 80 92 PRT Physcomitrella patens 80 Lys Ile Ala Lys Trp Arg Leu Thr Lys Trp Cys Ser Lys Asn Lys Lys 1 5 10 15 Thr Tyr Gln Met Thr His Val Ala Thr Thr Gln Ser Phe Arg Lys Asn 20 25 30 Glu Leu Ser Ile Lys Glu Arg Leu Ile Ala Ser Pro Phe Leu Ser Pro 35 40 45 His Lys Thr Leu Phe Thr Ser Gln Leu Arg Ile Lys Ala Ala Gln Thr 50 55 60 Asp Cys Lys Arg Leu Lys Ser Ala Gln Arg Val Pro Val Ile His Arg 65 70 75 80 Lys His Val Leu Ser Asp Leu Ser Glu Leu Gln Gln 85 90 81 289 DNA Physcomitrella patens CDS (2)..(289) 17_ck3_c03fwd 81 t caa gct act gtg ttg cca aat cca aat gtg aaa caa gcc tgt cga gtg 49 Gln Ala Thr Val Leu Pro Asn Pro Asn Val Lys Gln Ala Cys Arg Val 1 5 10 15 ttt cag ggg ggt tgt gtt gct cac ctg cac aag ctg ttg tcc atc gag 97 Phe Gln Gly Gly Cys Val Ala His Leu His Lys Leu Leu Ser Ile Glu 20 25 30 gct ggt tct cag gtt tta tat gta ggt gat cat att tat ggg gat att 145 Ala Gly Ser Gln Val Leu Tyr Val Gly Asp His Ile Tyr Gly Asp Ile 35 40 45 cta cga agc aag aaa gag tta gga tgg agg aca atg ctt gta gtg cca 193 Leu Arg Ser Lys Lys Glu Leu Gly Trp Arg Thr Met Leu Val Val Pro 50 55 60 gaa tta gcg gtc gag ctg gat tta ctc cat caa acc att aga act cgg 241 Glu Leu Ala Val Glu Leu Asp Leu Leu His Gln Thr Ile Arg Thr Arg 65 70 75 80 aag ggg att tcc gag ttg cgc aat caa cgt gat gaa ata gaa gat agt 289 Lys Gly Ile Ser Glu Leu Arg Asn Gln Arg Asp Glu Ile Glu Asp Ser 85 90 95 82 96 PRT Physcomitrella patens 82 Gln Ala Thr Val Leu Pro Asn Pro Asn Val Lys Gln Ala Cys Arg Val 1 5 10 15 Phe Gln Gly Gly Cys Val Ala His Leu His Lys Leu Leu Ser Ile Glu 20 25 30 Ala Gly Ser Gln Val Leu Tyr Val Gly Asp His Ile Tyr Gly Asp Ile 35 40 45 Leu Arg Ser Lys Lys Glu Leu Gly Trp Arg Thr Met Leu Val Val Pro 50 55 60 Glu Leu Ala Val Glu Leu Asp Leu Leu His Gln Thr Ile Arg Thr Arg 65 70 75 80 Lys Gly Ile Ser Glu Leu Arg Asn Gln Arg Asp Glu Ile Glu Asp Ser 85 90 95 83 566 DNA Physcomitrella patens CDS (1)..(516) 44_ck20_h07fwd 83 ttg ggc tct ggt aaa cac acc gcg gaa gtc atc atc ggc agt aac gga 48 Leu Gly Ser Gly Lys His Thr Ala Glu Val Ile Ile Gly Ser Asn Gly 1 5 10 15 tgt gtc aaa gtg aca tct gga atc acc gat ttg tcg tta ttg aaa aca 96 Cys Val Lys Val Thr Ser Gly Ile Thr Asp Leu Ser Leu Leu Lys Thr 20 25 30 act cag tct gga ttt gaa aag ttt gtc cgc gac cag ttc acc ata ttg 144 Thr Gln Ser Gly Phe Glu Lys Phe Val Arg Asp Gln Phe Thr Ile Leu 35 40 45 cca gac aca gat gag cgc atg cta gcc tca acc atc act ggc gtg tgg 192 Pro Asp Thr Asp Glu Arg Met Leu Ala Ser Thr Ile Thr Gly Val Trp 50 55 60 agt tac tcc ggc aag ccc gcg aat tac cag agg agt tgg gaa gcg gtg 240 Ser Tyr Ser Gly Lys Pro Ala Asn Tyr Gln Arg Ser Trp Glu Ala Val 65 70 75 80 aaa aaa gta ctt atg gac aca ttt ttc ggt tcg ccc ccc act ggt gtg 288 Lys Lys Val Leu Met Asp Thr Phe Phe Gly Ser Pro Pro Thr Gly Val 85 90 95 tat agt ccc tcc gtc cag cat act ctg tat caa atg gct aag gcc gta 336 Tyr Ser Pro Ser Val Gln His Thr Leu Tyr Gln Met Ala Lys Ala Val 100 105 110 cta gtc agg ttt cca gag atc gag aac ata cac ttg aac atg cca aac 384 Leu Val Arg Phe Pro Glu Ile Glu Asn Ile His Leu Asn Met Pro Asn 115 120 125 atc cat ttc cta cct gtt aac tta cct acg gtg ggc gtc aag ttc gag 432 Ile His Phe Leu Pro Val Asn Leu Pro Thr Val Gly Val Lys Phe Glu 130 135 140 aac gat gtc ttt ctt cca acc gat gaa ccc cat ggt tcg ata gaa gcc 480 Asn Asp Val Phe Leu Pro Thr Asp Glu Pro His Gly Ser Ile Glu Ala 145 150 155 160 aag ctc tcc cgg atg gaa att ttc cag tgc aag tta tgaaatcgtg 526 Lys Leu Ser Arg Met Glu Ile Phe Gln Cys Lys Leu 165 170 aggtctcatc gggaatcctt gaaggtatcg atgtgcggat 566 84 172 PRT Physcomitrella patens 84 Leu Gly Ser Gly Lys His Thr Ala Glu Val Ile Ile Gly Ser Asn Gly 1 5 10 15 Cys Val Lys Val Thr Ser Gly Ile Thr Asp Leu Ser Leu Leu Lys Thr 20 25 30 Thr Gln Ser Gly Phe Glu Lys Phe Val Arg Asp Gln Phe Thr Ile Leu 35 40 45 Pro Asp Thr Asp Glu Arg Met Leu Ala Ser Thr Ile Thr Gly Val Trp 50 55 60 Ser Tyr Ser Gly Lys Pro Ala Asn Tyr Gln Arg Ser Trp Glu Ala Val 65 70 75 80 Lys Lys Val Leu Met Asp Thr Phe Phe Gly Ser Pro Pro Thr Gly Val 85 90 95 Tyr Ser Pro Ser Val Gln His Thr Leu Tyr Gln Met Ala Lys Ala Val 100 105 110 Leu Val Arg Phe Pro Glu Ile Glu Asn Ile His Leu Asn Met Pro Asn 115 120 125 Ile His Phe Leu Pro Val Asn Leu Pro Thr Val Gly Val Lys Phe Glu 130 135 140 Asn Asp Val Phe Leu Pro Thr Asp Glu Pro His Gly Ser Ile Glu Ala 145 150 155 160 Lys Leu Ser Arg Met Glu Ile Phe Gln Cys Lys Leu 165 170 85 18 DNA Artificial sequence Sequencing primer 85 caggaaacag ctatgacc 18 86 19 DNA Artificial sequence Sequencing primer 86 ctaaagggaa caaaagctg 19 87 18 DNA Artificial sequence Sequencing primer 87 tgtaaaacga cggccagt 18 

1. An isolated nucleic acid molecule from a moss encoding a metabolic pathway (MP) protein, or a portion thereof.
 2. An isolated nuclei acid molecule wherein the moss is selected from Physcomitrella patens or Ceratodon purpureus.
 3. The isolated nucleic acid molecule of claim 1 or 2, wherein said nucleic acid molecule encodes an MP protein capable of performing an enzymatic step involved in the production of a fine chemical.
 4. The isolated nucleic acid molecule of any one of claims 1 to 3, wherein said nucleic acid molecule encodes an MP protein capable of performing an enzymatic step involved in the metabolism of amino acids, vitamins, cofactors, nutraceuticals, nucleotides and/or nucleosides.
 5. The isolated nucleic acid molecule of any one of claims 1 to 4, wherein said nucleic acid molecule encodes an MP protein assisting in the transmembrane transport.
 6. An isolated nucleic acid molecule from mosses selected from the group consisting of those sequences set forth in Appendix A, or a portion thereof.
 7. An isolated nucleic acid molecule which encodes a polypeptide sequence selected from the group consisting of those sequences set forth in Appendix B.
 8. An isolated nucleic acid molecule which encodes a naturally occurring allelic variant of a polypeptide selected from the group of amino acid sequences consisting of those sequences set forth in Appendix B.
 9. An isolated nucleic acid molecule comprising a nucleotide sequence which is at least 50% homologous to a nucleotide sequence selected from the group consisting of those sequences set forth in Appendix A, or a portion thereof.
 10. An isolated nucleic acid molecule comprising a fragment of at least 15 nucleotides of a nucleic acid comprising a nucleotide sequence selected from the group consisting of those sequences set forth in Appendix A.
 11. An isolated nucleic acid molecule which hybridizes to the nucleic acid molecule of any one of claims 1-10 under stringent conditions.
 12. An isolated nucleic acid molecule comprising the nucleic acid molecule of any one of claims 1-11 or a portion thereof and a nucleotide sequence encoding a heterologous polypeptide.
 13. A vector comprising the nucleic acid molecule of any one of claims 1-12.
 14. The vector of claim 13, which is an expression vector.
 15. A host cell transformed with the expression vector of claim
 14. 16. The host cell of claim 15, wherein said cell is a microorganism.
 17. The host cell of claim 15, wherein said cell belongs to the genus mosses or algae.
 18. The host cell of claim 15, wherein said cell is a plant cell.
 19. The host cell of any one of claims 15 to 18, wherein the expression of said nucleic acid molecule results in the modulation of the production of a fine chemical from said cell.
 20. The host cell of any one of claims 15 to 19, wherein the expression of said nucleic acid molecule results in the modulation of the production of amino acids, vitamins, cofactors, nutraceuticals, nucleotides and/or nucleosides from said cell.
 21. Descendants, seeds or reproducable cell material derived from a host cell of any one of claims 15 to
 20. 22. A method of producing a polypeptide comprising culturing the host cell of any one of claims 15 to 20 in an appropriate culture medium to, thereby, produce the polypeptide.
 23. An isolated MP protein from mosses or algae or a portion thereof.
 24. An isolated MP protein from microorganisms or fungi or a portion thereof.
 25. An isolated MP protein from plants or a portion thereof.
 26. The polypeptide of any one of claims 23 to 25, wherein said polypeptide is involved in the production of a fine chemical.
 27. The polypeptide of any one of claims 23 to 25, wherein said polypeptide is involved in assisting in transmembrane transport.
 28. An isolated polypeptide comprising an amino acid sequence selected from the group consisting of those sequences set forth in Appendix B.
 29. An isolated polypeptide comprising a naturally occurring allelic variant of a polypeptide comprising an amino acid sequence selected from the group consisting of those sequences set forth in Appendix B, or a portion thereof.
 30. The isolated polypeptide of any of claims 23 to 29, further comprising heterologous amino acid sequences.
 31. An isolated polypeptide which is encoded by a nucleic acid molecule comprising a nucleotide sequence which is at least 50% homologous to a nucleic acid selected from the group consisting of those sequences set forth in Appendix A.
 32. An isolated polypeptide comprising an amino acid sequence which is at least 50% homologous to an amino acid sequence selected from the group consisting of those sequences set forth in Appendix B.
 33. An antibody specifically binding to a MP protein of any one of claims 23 to 32 or a portion thereof.
 34. Test kit comprising a nucleic acid molecule of any one of claims 1 to 12, a portion and/or a complement thereof used as probe or primer for identifying and/or cloning further nucleic acid molecules involved in the production of amino acids, vitamins, cofactors, nucloetides and/or nucleosides or assisting in transmembrane transport in other cell types or organisms.
 35. Test kit comprising an MP protein-antibody of claim 33 for identifying and/or purifying further MP protein molecules or fragments thereof in other cell types or organisms.
 36. A method for producing a fine chemical, comprising culturing a cell containing a vector of claim 13 or 14 such that the fine chemical is produced.
 37. The method of claim 36, wherein said method further comprises the step of recovering the fine chemical from said culture.
 38. The method of claim 36 or 37, wherein said method further comprises the step of transforming said cell with the vector of claim 13 or 14 to result in a cell containing said vector.
 39. The method of any one of claims 36 to 38, wherein said cell is a microorganism.
 40. The method of any one of claims 36 to 38, wherein said cell belongs to the genus Corynebacterium or Brevibacterium.
 41. The method of any one of claims 36 to 38, wherein said cell belongs to the genus mosses or algae.
 42. The method of any one of claims 36 to 38, wherein said cell is a plant cell.
 43. The method of any one of claims 36 to 42, wherein expression of the nucleic acid molecule from said vector results in modulation of the production of said fine chemical.
 44. The method of claim 43, wherein said fine chemical is selected from the group consisting of amino acids, vitamins, cofactors, nucloetides and/or nucleosides.
 45. A method for producing a fine chemical, comprising culturing a cell whose genomic DNA has been altered by the inclusion of a nucleic acid molecule of any one of claims 1-12.
 46. A method of claim 45, comprising culturing a cell whose membrane has been altered by the inclusion of a polypeptide of any one of claims 22 to
 32. 47. A fine chemical produced by a method of any one of claims 36 to
 46. 48. Use of a fine chemical of claim 47 or a polypeptide of any one of claims 22 to 32 for the production of another fine chemical. 